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138-41-0,MFCD00007938
Catalog No.:AA0017QE

138-41-0 | 4-Carboxybenzenesulfonamide

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Purity
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Price(USD)
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5g
95%
in stock  
$18.00   $13.00
- +
25g
98%
in stock  
$18.00   $13.00
- +
100g
98%
in stock  
$58.00   $41.00
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500g
95%
in stock  
$254.00   $178.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0017QE
Chemical Name:
4-Carboxybenzenesulfonamide
CAS Number:
138-41-0
Molecular Formula:
C7H7NO4S
Molecular Weight:
201.1998
MDL Number:
MFCD00007938
SMILES:
OC(=O)c1ccc(cc1)S(=O)(=O)N
Properties
Computed Properties
 
Complexity:
284  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  
XLogP3:
0.5  

Upstream Synthesis Route

[1]AmericanChemicalJournal,1896,vol.18,p.163,165

[2]YakugakuZasshi,1949,vol.69,p.417

[3]Chem.Abstr.,1950,p.1924

[4]Patent:WO2005/34885,2005,A1,.Locationinpatent:Page/Pagecolumn36

[1]AmericanChemicalJournal,1896,vol.18,p.163,165

[1]Patent:CN105801455,2016,A,.Locationinpatent:Paragraph0048

[2]Patent:US2004/58977,2004,A1,.Locationinpatent:Page/Pagecolumn8;14

[3]AmericanChemicalJournal,1885,vol.7,p.147

[4]JustusLiebigsAnnalenderChemie,1875,vol.178,p.284

[5]JournaloftheChemicalSociety,1951,p.1877,1880

[6]BollettinoChimicoFarmaceutico,1956,vol.95,p.287,290

[7]Rep.Gov.chem.ind.Res.Inst.Tokyo,1950,vol.45,p.295,297

[8]Chem.Abstr.,1952,p.4269

[9]BioorganicandMedicinalChemistry,2014,vol.22,#6,p.1873-1882

[10]Patent:CN105693565,2016,A,.Locationinpatent:Paragraph0044;0045;0046

[11]BioorganicandMedicinalChemistry,2017,vol.25,#3,p.1286-1293

[1]JournalofMedicinalChemistry,1988,vol.31,#9,p.1762-1767

[2]VerslagvandeGewoneVergaderingvandeAfdelingNatuurkunde,KoninklijkeNederlandseAkademievanWetenschappen,vol.32,p.15

[3]Chem.Zentralbl.,1923,vol.94,#III,p.302

[4]JournalofOrganicChemistry,1968,vol.33,#9,p.3610-3618

[5]Patent:US5935990,1999,A,

[1]Synthesis,2000,#5,p.646-650

[2]JournalofOrganicChemistry,1968,vol.33,#9,p.3610-3618

Downstream Synthesis Route

[1]JournaloftheChemicalSociety,1951,p.1877,1880

[2]MagneticResonanceinChemistry,1989,vol.27,p.585-591

[1]JournaloftheAmericanChemicalSociety,2006,vol.128,p.3273-3280

[2]JournalofMedicinalChemistry,2010,vol.53,p.4555-4559

[3]EuropeanJournalofMedicinalChemistry,2018,vol.156,p.430-443

[4]Patent:CN110903262,2020,A.Locationinpatent:Paragraph0059-0063

[5]Patent:WO2009/115515,2009,A1.Locationinpatent:Page/Pagecolumn26

[6]AdvancedSynthesisandCatalysis,2020,vol.362,p.561-571

[7]BollettinoChimicoFarmaceutico,1997,vol.136,p.244-249

[8]Patent:WO2007/23186,2007,A1.Locationinpatent:Page/Pagecolumn49

[9]Tetrahedron,1993,vol.49,p.11329-11340

[10],1949,vol.39,p.109,112,113

[11]KagakuKenkyushoHokoku,1950,vol.26,p.301,302

[12]JournalofMedicinalChemistry,2005,vol.48,p.2121-2125

[13]BioorganicandMedicinalChemistry,2009,vol.17,p.3028-3036

[14]BioorganicandMedicinalChemistry,2014,vol.22,p.1873-1882

[15]ACSMedicinalChemistryLetters,2017,vol.8,p.792-796

[16]EuropeanJournalofMedicinalChemistry,2018,vol.157,p.28-36

[17]BioorganicandMedicinalChemistry,2019,vol.27,p.1087-1098

[18]EuropeanJournalofMedicinalChemistry,2020,vol.193

[1]JournalofMedicinalChemistry,1988,vol.31,p.1762-1767

[2]VerslagvandeGewoneVergaderingvandeAfdelingNatuurkunde,KoninklijkeNederlandseAkademievanWetenschappen,vol.32,p.15    ChemischesZentralblatt,1923,vol.94,p.302

[3]JournalofOrganicChemistry,1968,vol.33,p.3610-3618

[4]Patent:US5935990,1999,A

[1]Patent:CN105801455,2016,A.Locationinpatent:Paragraph0048

[2]Patent:US2004/58977,2004,A1.Locationinpatent:Page/Pagecolumn8;14

[3]AdvancedSynthesisandCatalysis,2020,vol.362,p.561-571

[4]AmericanChemicalJournal,1885,vol.7,p.147

[5]JustusLiebigsAnnalenderChemie,1875,vol.178,p.284

[6]JournaloftheChemicalSociety,1951,p.1877,1880

[7]BioorganicandMedicinalChemistry,2014,vol.22,p.1873-1882

[8]Patent:CN105693565,2016,A.Locationinpatent:Paragraph0044;0045;0046

[9]BioorganicandMedicinalChemistry,2017,vol.25,p.1286-1293

[10]EuropeanJournalofMedicinalChemistry,2020,vol.193

[1]Patent:JP5676853,2015,B2.Locationinpatent:Paragraph0072-0074

[2]JournaloftheAmericanChemicalSociety,1994,vol.116,p.5057-5062

[3]Chemistry-AnAsianJournal,2012,vol.7,p.1567-1571

[4]Chemistry-AEuropeanJournal,2004,vol.10,p.2375-2385

[5]JournalofMedicinalChemistry,2015,vol.58,p.4039-4045

[6]ChemicalCommunications,2015,vol.51,p.17265-17268

[7]AngewandteChemie-InternationalEdition,2005,vol.44,p.5480-5483

[8]BioorganicandMedicinalChemistryLetters,1996,vol.6,p.559-564

[9]AngewandteChemie-InternationalEdition,2014,vol.53,p.4231-4235    Angew.Chem.,2014,vol.126,p.4315-4320,6

[10]JournaloftheAmericanChemicalSociety,2015,vol.137,p.7286-7289

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Title: Polymers of 2-methacryloyloxyethyl phosphorylcholine truly work as cell membrane mimic?

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Tags:138-41-0 Molecular Formula|138-41-0 MDL|138-41-0 SMILES|138-41-0 4-Carboxybenzenesulfonamide |Organic_Building_Blocks