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98-68-0,MFCD00007446
Catalog No.:AA00340L

98-68-0 | 4-Methoxybenzenesulfonyl chloride

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
98%
in stock  
$7.00   $5.00
- +
25g
98%
in stock  
$16.00   $11.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00340L
Chemical Name:
4-Methoxybenzenesulfonyl chloride
CAS Number:
98-68-0
Molecular Formula:
C7H7ClO3S
Molecular Weight:
206.6467
MDL Number:
MFCD00007446
SMILES:
COc1ccc(cc1)S(=O)(=O)Cl
NSC Number:
403292
Properties
Properties
 
BP:
173°C at 760 mmHg  
Form:
Solid  
MP:
39-42 °C  
Stability:
Moisture Sensitive  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
224  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
2  
XLogP3:
1.5  

Upstream Synthesis Route

[1]AngewandteChemie-InternationalEdition,2015,vol.54,#40,p.11775-11779

[2]Angew.Chem.,2015,vol.254,#40,p.11775-11779,5

[1]MarineDrugs,2016,vol.14,#5,

[2]RSCAdvances,2016,vol.6,#96,p.93476-93485

[3]Tetrahedron,2017,vol.73,#49,p.6871-6879

[4]JournalofOrganicChemistry,2014,vol.79,#1,p.328-338

[5]BioorganicandMedicinalChemistry,2014,vol.22,#17,p.4629-4636

[6]BioorganicandMedicinalChemistry,2015,vol.23,#13,p.3397-3407

[7]ArchivderPharmazie,2017,vol.350,#11,

[8]LettersinDrugDesignandDiscovery,2018,vol.15,#12,p.1288-1298

[9]JournalofInorganicBiochemistry,2013,vol.127,p.188-202

[10]OrganicLetters,2018,vol.20,#13,p.4023-4027

[11]JustusLiebigsAnnalenderChemie,1959,vol.622,p.133,147

[12]BulletindelaSocieteChimiquedeFrance,1964,p.248-250

[13]Synthesis,1993,#5,p.490-496

[14]AntimicrobialAgentsandChemotherapy,2002,vol.46,#8,p.2450-2457

[15]BioorganicandMedicinalChemistry,2009,vol.17,#21,p.7429-7434

[16]EuropeanJournalofMedicinalChemistry,2011,vol.46,#11,p.5540-5548

[17]BioorganicandMedicinalChemistry,2012,vol.20,#9,p.2837-2844

[18]Chemistry-AEuropeanJournal,2012,vol.18,#6,p.1582-1585

[19]BioorganicandMedicinalChemistry,2012,vol.20,#9,p.2837-2844

[20]OrganicandBiomolecularChemistry,2012,vol.10,#37,p.7479-7482

[21]GreenChemistry,2014,vol.16,#9,p.4106-4109

[22]GreenChemistry,2016,vol.18,#9,p.2609-2613

[23]GreenChemistry,2017,vol.19,#1,p.112-116

[24]GreenChemistry,2017,vol.19,#24,p.5794-5799

[25]ChemicalCommunications,2014,vol.50,#86,p.13121-13123

[26]ACSCombinatorialScience,2015,vol.17,#11,p.658-662

[27]OrganicandBiomolecularChemistry,2015,vol.14,#2,p.590-597

[28]EuropeanJournalofOrganicChemistry,2016,vol.2016,#5,p.910-912

[29]OrganicandBiomolecularChemistry,2016,vol.14,#10,p.2824-2827

[30]Chemistry-AnAsianJournal,2016,vol.11,#4,p.478-481

[31]MedicinalChemistryResearch,2016,vol.25,#7,p.1425-1432

[32]MedicinalChemistryResearch,2016,vol.25,#8,p.1590-1607

[33]OrganicandBiomolecularChemistry,2016,vol.14,#46,p.10833-10839

[34]EuropeanJournalofOrganicChemistry,2017,vol.2017,#24,p.3512-3515

[35]JournalofOrganicChemistry,2017,vol.82,#13,p.6764-6769

[36]OrganicandBiomolecularChemistry,2017,vol.15,#37,p.7819-7823

[37]GreenChemistry,2017,vol.19,#24,p.5940-5948

[38]NewJournalofChemistry,2018,vol.42,#13,p.10953-10957

[39]ChemicalCommunications,2018,vol.54,#81,p.11471-11474

[40]JournalofOrganicChemistry,2018,vol.83,#23,p.14419-14430

[1]BioorganicandMedicinalChemistryLetters,2009,vol.19,#24,p.7003-7006

[1]JournalofMedicinalChemistry,1992,vol.35,#13,p.2496-2497

[2]Patent:WO2006/76511,2006,A1,.Locationinpatent:Page/Pagecolumn16

[3]Patent:WO2006/76630,2006,A1,.Locationinpatent:Page/Pagecolumn14

[4]Patent:US2006/293367,2006,A1,.Locationinpatent:Page/Pagecolumn2

[1]Patent:US5723490,1998,A,

Downstream Synthesis Route

[1]MarineDrugs,2016,vol.14

[2]RSCAdvances,2016,vol.6,p.93476-93485

[3]Tetrahedron,2017,vol.73,p.6871-6879

[4]JournalofOrganicChemistry,2014,vol.79,p.328-338

[5]BioorganicandMedicinalChemistry,2014,vol.22,p.4629-4636

[6]BioorganicandMedicinalChemistry,2015,vol.23,p.3397-3407

[7]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.6951-6955

[8]ArchivderPharmazie,2017,vol.350

[9]Lettersindrugdesignanddiscovery,2018,vol.15,p.1288-1298

[10]Patent:WO2019/108824,2019,A1.Locationinpatent:Paragraph0328-0331;0327

[11]JournalofInorganicBiochemistry,2013,vol.127,p.188-202

[12]OrganicLetters,2018,vol.20,p.4023-4027

[13]JustusLiebigsAnnalenderChemie,1959,vol.622,p.133,147

[14]BulletindelaSocieteChimiquedeFrance,1964,p.248-250

[15]Synthesis,1993,p.490-496

[16]AntimicrobialAgentsandChemotherapy,2002,vol.46,p.2450-2457

[17]BioorganicandMedicinalChemistry,2009,vol.17,p.7429-7434

[18]EuropeanJournalofMedicinalChemistry,2011,vol.46,p.5540-5548

[19]Chemistry-AEuropeanJournal,2012,vol.18,p.1582-1585

[20]BioorganicandMedicinalChemistry,2012,vol.20,p.2837-2844

[21]OrganicandBiomolecularChemistry,2012,vol.10,p.7479-7482

[22]GreenChemistry,2014,vol.16,p.4106-4109

[23]ChemicalCommunications,2014,vol.50,p.13121-13123

[24]ACSCombinatorialScience,2015,vol.17,p.658-662

[25]OrganicandBiomolecularChemistry,2015,vol.14,p.590-597

[26]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.910-912

[27]OrganicandBiomolecularChemistry,2016,vol.14,p.2824-2827

[28]Chemistry-AnAsianJournal,2016,vol.11,p.478-481

[29]MedicinalChemistryResearch,2016,vol.25,p.1425-1432

[30]MedicinalChemistryResearch,2016,vol.25,p.1590-1607

[31]OrganicandBiomolecularChemistry,2016,vol.14,p.10833-10839

[32]EuropeanJournalofOrganicChemistry,2017,vol.2017,p.3512-3515

[33]JournalofOrganicChemistry,2017,vol.82,p.6764-6769

[34]OrganicandBiomolecularChemistry,2017,vol.15,p.7819-7823

[35]GreenChemistry,2017,vol.19,p.5940-5948

[36]NewJournalofChemistry,2018,vol.42,p.10953-10957

[37]ChemicalCommunications,2018,vol.54,p.11471-11474

[38]JournalofOrganicChemistry,2018,vol.83,p.14419-14430

[39]Chemistry-AEuropeanJournal,2018,vol.24,p.19156-19161

[40]AdvancedSynthesisandCatalysis,2019,vol.361,p.2280-2285

[41]AdvancedSynthesisandCatalysis,2019,vol.361,p.4575-4580

[42]MedicinalChemistryResearch,2020

[43]BioorganicChemistry,2020,vol.94

[44]Molecules,2020,vol.25

[45]OrganicLetters,2020,vol.22,p.1818-1824

[1]Journalofmedicinalandpharmaceuticalchemistry,1962,vol.5,p.247-257

[1]IlFarmaco,1992,vol.47,p.265-274

3034-38-6    98-68-0   
1-(p-methoxybenzenesulfonyl)-4-nitroimidazole 

[1]Tetrahedron,1994,vol.50,p.5741-5752

[1]JournaloftheChemicalSociety.PerkintransactionsII,1991,p.1175-1179

[2]JournaloftheChemicalSociety.PerkintransactionsII,1991,p.1175-1179

Literature

Title: Ethyl 3-[7-eth-oxy-6-(4-meth-oxy-benzene-sulfonamido)-2H-indazol-2-yl]propano-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20120401

Title: Application of the dissociative electron transfer theory and its extension to the case of in-cage interactions in the electrochemical reduction of arene sulfonyl chlorides.

Journal: Physical chemistry chemical physics : PCCP 20120107

Title: 3-Hy-droxy-2-(4-meth-oxy-benzene-sulfonamido)-butanoic acid.

Journal: Acta crystallographica. Section E, Structure reports online 20111201

Title: N-(2-Formyl-phen-yl)-4-meth-oxy-N-(4-meth-oxy-phenyl-sulfon-yl)benzene-sulfonamide.

Journal: Acta crystallographica. Section E, Structure reports online 20111201

Title: 4-[(4-Meth-oxy-benzene-sulfonamido)-meth-yl]cyclo-hexane-1-carb-oxy-lic acid.

Journal: Acta crystallographica. Section E, Structure reports online 20110901

Title: 4-(4-Meth-oxy-benzene-sulfonamido)-benzoic acid.

Journal: Acta crystallographica. Section E, Structure reports online 20110701

Title: Cucurbit[7]uril: surfactant host-guest complexes in equilibrium with micellar aggregates.

Journal: Chemphyschem : a European journal of chemical physics and physical chemistry 20110509

Title: N-Cyclo-hexyl-4-meth-oxy-benzene-sulfonamide.

Journal: Acta crystallographica. Section E, Structure reports online 20110401

Title: (2S)-3-Carbamoyl-2-(4-meth-oxy-benzene-sulfonamido)-propanoic acid.

Journal: Acta crystallographica. Section E, Structure reports online 20101001

Title: Novel reagents for quantitative analysis of valiolamine in biological samples by high-performance liquid chromatography with pre-column UV derivatization.

Journal: Talanta 20100615

Title: 1-(4-Methoxy-phenyl-sulfon-yl)-5-methyl-5-phenyl-imidazolidine-2,4-dione.

Journal: Acta crystallographica. Section E, Structure reports online 20090601

Title: 4-Meth-oxy-N-[6-methyl-2,3-dihydro-1,3-benzothia-zol-2-yl-idene]benzene-sulfonamide.

Journal: Acta crystallographica. Section E, Structure reports online 20080101

Title: New insights in cyclodextrin: surfactant mixed systems from the use of neutral and anionic cyclodextrin derivatives.

Journal: The journal of physical chemistry. B 20071108

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Tags:98-68-0 Molecular Formula|98-68-0 MDL|98-68-0 SMILES|98-68-0 4-Methoxybenzenesulfonyl chloride
Catalog No.: AA00340L
98-68-0,MFCD00007446
98-68-0 | 4-Methoxybenzenesulfonyl chloride
Pack Size： 10g
Purity： 98%
in stock
$7.00 $5.00
Pack Size： 25g
Purity： 98%
in stock
$16.00 $11.00
Quantity
- +
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Technical Information
Catalog Number: AA00340L
Chemical Name: 4-Methoxybenzenesulfonyl chloride
CAS Number: 98-68-0
Molecular Formula: C7H7ClO3S
Molecular Weight: 206.6467
MDL Number: MFCD00007446
SMILES: COc1ccc(cc1)S(=O)(=O)Cl
NSC Number: 403292
Properties
BP: 173°C at 760 mmHg  
Form: Solid  
MP: 39-42 °C  
Stability: Moisture Sensitive  
Storage: Inert atmosphere;2-8℃;  
Complexity: 224  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 2  
XLogP3: 1.5  
Upstream Synthesis Route
98-68-0    10557-27-4 

[1]AngewandteChemie-InternationalEdition,2015,vol.54,#40,p.11775-11779

[2]Angew.Chem.,2015,vol.254,#40,p.11775-11779,5

98-68-0    1950-68-1 

[1]MarineDrugs,2016,vol.14,#5,

[2]RSCAdvances,2016,vol.6,#96,p.93476-93485

[3]Tetrahedron,2017,vol.73,#49,p.6871-6879

[4]JournalofOrganicChemistry,2014,vol.79,#1,p.328-338

[5]BioorganicandMedicinalChemistry,2014,vol.22,#17,p.4629-4636

[6]BioorganicandMedicinalChemistry,2015,vol.23,#13,p.3397-3407

[7]ArchivderPharmazie,2017,vol.350,#11,

[8]LettersinDrugDesignandDiscovery,2018,vol.15,#12,p.1288-1298

[9]JournalofInorganicBiochemistry,2013,vol.127,p.188-202

[10]OrganicLetters,2018,vol.20,#13,p.4023-4027

[11]JustusLiebigsAnnalenderChemie,1959,vol.622,p.133,147

[12]BulletindelaSocieteChimiquedeFrance,1964,p.248-250

[13]Synthesis,1993,#5,p.490-496

[14]AntimicrobialAgentsandChemotherapy,2002,vol.46,#8,p.2450-2457

[15]BioorganicandMedicinalChemistry,2009,vol.17,#21,p.7429-7434

[16]EuropeanJournalofMedicinalChemistry,2011,vol.46,#11,p.5540-5548

[17]BioorganicandMedicinalChemistry,2012,vol.20,#9,p.2837-2844

[18]Chemistry-AEuropeanJournal,2012,vol.18,#6,p.1582-1585

[19]BioorganicandMedicinalChemistry,2012,vol.20,#9,p.2837-2844

[20]OrganicandBiomolecularChemistry,2012,vol.10,#37,p.7479-7482

[21]GreenChemistry,2014,vol.16,#9,p.4106-4109

[22]GreenChemistry,2016,vol.18,#9,p.2609-2613

[23]GreenChemistry,2017,vol.19,#1,p.112-116

[24]GreenChemistry,2017,vol.19,#24,p.5794-5799

[25]ChemicalCommunications,2014,vol.50,#86,p.13121-13123

[26]ACSCombinatorialScience,2015,vol.17,#11,p.658-662

[27]OrganicandBiomolecularChemistry,2015,vol.14,#2,p.590-597

[28]EuropeanJournalofOrganicChemistry,2016,vol.2016,#5,p.910-912

[29]OrganicandBiomolecularChemistry,2016,vol.14,#10,p.2824-2827

[30]Chemistry-AnAsianJournal,2016,vol.11,#4,p.478-481

[31]MedicinalChemistryResearch,2016,vol.25,#7,p.1425-1432

[32]MedicinalChemistryResearch,2016,vol.25,#8,p.1590-1607

[33]OrganicandBiomolecularChemistry,2016,vol.14,#46,p.10833-10839

[34]EuropeanJournalofOrganicChemistry,2017,vol.2017,#24,p.3512-3515

[35]JournalofOrganicChemistry,2017,vol.82,#13,p.6764-6769

[36]OrganicandBiomolecularChemistry,2017,vol.15,#37,p.7819-7823

[37]GreenChemistry,2017,vol.19,#24,p.5940-5948

[38]NewJournalofChemistry,2018,vol.42,#13,p.10953-10957

[39]ChemicalCommunications,2018,vol.54,#81,p.11471-11474

[40]JournalofOrganicChemistry,2018,vol.83,#23,p.14419-14430

98-68-0    927-74-2    23418-85-1 

[1]BioorganicandMedicinalChemistryLetters,2009,vol.19,#24,p.7003-7006

78750-68-2    98-68-0    141430-65-1 

[1]JournalofMedicinalChemistry,1992,vol.35,#13,p.2496-2497

[2]Patent:WO2006/76511,2006,A1,.Locationinpatent:Page/Pagecolumn16

[3]Patent:WO2006/76630,2006,A1,.Locationinpatent:Page/Pagecolumn14

[4]Patent:US2006/293367,2006,A1,.Locationinpatent:Page/Pagecolumn2

4248-19-5    98-68-0    148017-28-1 

[1]Patent:US5723490,1998,A,

Downstream Synthesis Route
98-68-0    1950-68-1 

[1]MarineDrugs,2016,vol.14

[2]RSCAdvances,2016,vol.6,p.93476-93485

[3]Tetrahedron,2017,vol.73,p.6871-6879

[4]JournalofOrganicChemistry,2014,vol.79,p.328-338

[5]BioorganicandMedicinalChemistry,2014,vol.22,p.4629-4636

[6]BioorganicandMedicinalChemistry,2015,vol.23,p.3397-3407

[7]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.6951-6955

[8]ArchivderPharmazie,2017,vol.350

[9]Lettersindrugdesignanddiscovery,2018,vol.15,p.1288-1298

[10]Patent:WO2019/108824,2019,A1.Locationinpatent:Paragraph0328-0331;0327

[11]JournalofInorganicBiochemistry,2013,vol.127,p.188-202

[12]OrganicLetters,2018,vol.20,p.4023-4027

[13]JustusLiebigsAnnalenderChemie,1959,vol.622,p.133,147

[14]BulletindelaSocieteChimiquedeFrance,1964,p.248-250

[15]Synthesis,1993,p.490-496

[16]AntimicrobialAgentsandChemotherapy,2002,vol.46,p.2450-2457

[17]BioorganicandMedicinalChemistry,2009,vol.17,p.7429-7434

[18]EuropeanJournalofMedicinalChemistry,2011,vol.46,p.5540-5548

[19]Chemistry-AEuropeanJournal,2012,vol.18,p.1582-1585

[20]BioorganicandMedicinalChemistry,2012,vol.20,p.2837-2844

[21]OrganicandBiomolecularChemistry,2012,vol.10,p.7479-7482

[22]GreenChemistry,2014,vol.16,p.4106-4109

[23]ChemicalCommunications,2014,vol.50,p.13121-13123

[24]ACSCombinatorialScience,2015,vol.17,p.658-662

[25]OrganicandBiomolecularChemistry,2015,vol.14,p.590-597

[26]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.910-912

[27]OrganicandBiomolecularChemistry,2016,vol.14,p.2824-2827

[28]Chemistry-AnAsianJournal,2016,vol.11,p.478-481

[29]MedicinalChemistryResearch,2016,vol.25,p.1425-1432

[30]MedicinalChemistryResearch,2016,vol.25,p.1590-1607

[31]OrganicandBiomolecularChemistry,2016,vol.14,p.10833-10839

[32]EuropeanJournalofOrganicChemistry,2017,vol.2017,p.3512-3515

[33]JournalofOrganicChemistry,2017,vol.82,p.6764-6769

[34]OrganicandBiomolecularChemistry,2017,vol.15,p.7819-7823

[35]GreenChemistry,2017,vol.19,p.5940-5948

[36]NewJournalofChemistry,2018,vol.42,p.10953-10957

[37]ChemicalCommunications,2018,vol.54,p.11471-11474

[38]JournalofOrganicChemistry,2018,vol.83,p.14419-14430

[39]Chemistry-AEuropeanJournal,2018,vol.24,p.19156-19161

[40]AdvancedSynthesisandCatalysis,2019,vol.361,p.2280-2285

[41]AdvancedSynthesisandCatalysis,2019,vol.361,p.4575-4580

[42]MedicinalChemistryResearch,2020

[43]BioorganicChemistry,2020,vol.94

[44]Molecules,2020,vol.25

[45]OrganicLetters,2020,vol.22,p.1818-1824

52838-39-8    98-68-0    34243-14-6 

[1]Journalofmedicinalandpharmaceuticalchemistry,1962,vol.5,p.247-257

23031-78-9    98-68-0    142503-62-6 

[1]IlFarmaco,1992,vol.47,p.265-274

3034-38-6    98-68-0   
1-(p-methoxybenzenesulfonyl)-4-nitroimidazole 

[1]Tetrahedron,1994,vol.50,p.5741-5752

67-56-1    98-68-0    5857-42-1    6214-19-3 

[1]JournaloftheChemicalSociety.PerkintransactionsII,1991,p.1175-1179

[2]JournaloftheChemicalSociety.PerkintransactionsII,1991,p.1175-1179

Literature fold

Title: Ethyl 3-[7-eth-oxy-6-(4-meth-oxy-benzene-sulfonamido)-2H-indazol-2-yl]propano-ate.

Journal: Acta crystallographica. Section E, Structure reports online20120401

Title: Application of the dissociative electron transfer theory and its extension to the case of in-cage interactions in the electrochemical reduction of arene sulfonyl chlorides.

Journal: Physical chemistry chemical physics : PCCP20120107

Title: 3-Hy-droxy-2-(4-meth-oxy-benzene-sulfonamido)-butanoic acid.

Journal: Acta crystallographica. Section E, Structure reports online20111201

Title: N-(2-Formyl-phen-yl)-4-meth-oxy-N-(4-meth-oxy-phenyl-sulfon-yl)benzene-sulfonamide.

Journal: Acta crystallographica. Section E, Structure reports online20111201

Title: 4-[(4-Meth-oxy-benzene-sulfonamido)-meth-yl]cyclo-hexane-1-carb-oxy-lic acid.

Journal: Acta crystallographica. Section E, Structure reports online20110901

Title: 4-(4-Meth-oxy-benzene-sulfonamido)-benzoic acid.

Journal: Acta crystallographica. Section E, Structure reports online20110701

Title: Cucurbit[7]uril: surfactant host-guest complexes in equilibrium with micellar aggregates.

Journal: Chemphyschem : a European journal of chemical physics and physical chemistry20110509

Title: N-Cyclo-hexyl-4-meth-oxy-benzene-sulfonamide.

Journal: Acta crystallographica. Section E, Structure reports online20110401

Title: (2S)-3-Carbamoyl-2-(4-meth-oxy-benzene-sulfonamido)-propanoic acid.

Journal: Acta crystallographica. Section E, Structure reports online20101001

Title: Novel reagents for quantitative analysis of valiolamine in biological samples by high-performance liquid chromatography with pre-column UV derivatization.

Journal: Talanta20100615

Title: 1-(4-Methoxy-phenyl-sulfon-yl)-5-methyl-5-phenyl-imidazolidine-2,4-dione.

Journal: Acta crystallographica. Section E, Structure reports online20090601

Title: 4-Meth-oxy-N-[6-methyl-2,3-dihydro-1,3-benzothia-zol-2-yl-idene]benzene-sulfonamide.

Journal: Acta crystallographica. Section E, Structure reports online20080101

Title: New insights in cyclodextrin: surfactant mixed systems from the use of neutral and anionic cyclodextrin derivatives.

Journal: The journal of physical chemistry. B20071108

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