721-04-0,MFCD00156689
Catalog No.:AA00FE6I

721-04-0 | 2-Phenoxyacetophenone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$32.00   $23.00
- +
1g
98%
in stock  
$102.00   $72.00
- +
5g
98%
in stock  
$296.00   $207.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00FE6I
Chemical Name:
2-Phenoxyacetophenone
CAS Number:
721-04-0
Molecular Formula:
C14H12O2
Molecular Weight:
212.2439
MDL Number:
MFCD00156689
SMILES:
O=C(c1ccccc1)COc1ccccc1
NSC Number:
7586
Properties
Computed Properties
 
Complexity:
213  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.7  

Downstream Synthesis Route

[1]Chemistry-AEuropeanJournal,2020,vol.26,p.3641-3646

[2]JournaloftheAmericanChemicalSociety,2020,vol.142,p.4037-4050

[3]GreenChemistry,2016,vol.18,p.6229-6235

[4]DaltonTransactions,2017,vol.46,p.11884-11889

[5]GreenChemistry,2019,vol.21,p.2005-2014

[6]CatalysisToday,2016,vol.269,p.40-47

[7]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[8]ChemicalCommunications,2015,vol.51,p.4028-4031

[9]ACSCatalysis,2016,vol.6,p.1316-1328

[10]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12554-12555

[11]TetrahedronLetters,2010,vol.51,p.6418-6421

[12]ChemicalCommunications,2019,vol.55,p.13144-13147

[13]GreenChemistry,2020,vol.22,p.248-255

[14]Patent:US2016/52949,2016,A1.Locationinpatent:Paragraph0101

[15]GreenChemistry,2014,vol.16,p.2432-2437

[16]JournaloftheAmericanChemicalSociety,1958,vol.80,p.202

[17]JournaloftheChemicalSociety,1960,p.3521-3527

[18]JournaloftheChemicalSociety.PerkintransactionsII,1978,p.1135-1144

[19]ZeitschriftfurPhysikalischeChemie(Leipzig),1990,vol.271,p.927-930

[20]JournalofOrganicChemistry,2006,vol.71,p.7035-7044

[21]JournalofOrganicChemistry,2002,vol.67,p.7937-7945

[22]Tetrahedron,2008,vol.64,p.3867-3876

[23]JournalofOrganicChemistry,2011,vol.76,p.1883-1886

[24]ChemicalCommunications,2015,vol.51,p.12212-12215

[25]GreenChemistry,2015,vol.17,p.5009-5018

[26]GreenChemistry,2016,vol.18,p.2029-2036

[27]GreenChemistry,2016,vol.18,p.6545-6555

[28]GreenChemistry,2019,vol.21,p.1974-1981

[29]GreenChemistry,2019,vol.21,p.6707-6716

3598-14-9   
phenylmagnesiumbromide 
  721-04-0 

[1]JournaloftheAmericanChemicalSociety,1938,vol.60,p.1148,1150

[1]GreenChemistry,2016,vol.18,p.6229-6235

[2]GreenChemistry,2017,vol.19,p.4538-4543

[3]DaltonTransactions,2017,vol.46,p.11884-11889

[4]GreenChemistry,2019,vol.21,p.2005-2014

[5]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12554-12555

[6]ChemicalCommunications,2019,vol.55,p.13144-13147

[7]SyntheticCommunications,1996,vol.26,p.301-305

[8]Chemistry-AEuropeanJournal,2020,vol.26,p.10402-10405

[9]JournalofOrganicChemistry,2014,vol.79,p.6153-6163

[10]ACSCatalysis,2019,vol.9,p.11341-11349

[11]SyntheticCommunications,2009,vol.39,p.4079-4087

[12]GreenChemistry,2017,vol.19,p.702-706

[13]BioorganicandMedicinalChemistry,1998,vol.6,p.825-832

[14]GreenChemistry,2013,vol.15,p.768-774

[15]ACSCatalysis,2016,vol.6,p.1316-1328

[16]Patent:US2016/52949,2016,A1.Locationinpatent:Paragraph0100

[17]GreenChemistry,2020,vol.22,p.248-255

[18]BioorganicandMedicinalChemistryLetters,1998,vol.8,p.2773-2776

[19]CatalysisToday,2016,vol.269,p.40-47

[20]OrganicLetters,2020,vol.22,p.6055-6060

[21]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[22]TetrahedronLetters,2016,vol.57,p.3024-3028

[23]BioorganicandMedicinalChemistry,2007,vol.15,p.7337-7343

[24]Tetrahedron,1999,vol.55,p.12699-12710

[25]Patent:US6392089,2002,B1.Locationinpatent:Pagecolumn26

[26]TetrahedronLetters,2010,vol.51,p.6418-6421

[27]Chemistry-AEuropeanJournal,2020,vol.26,p.3641-3646

[28]ChemicalBiologyandDrugDesign,2012,vol.80,p.591-597

[29]GreenChemistry,2014,vol.16,p.2432-2437

[30]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1999,vol.38,p.1108-1110

[31]Tetrahedron,2008,vol.64,p.3867-3876

[32]JournalofOrganicChemistry,2005,vol.70,p.2720-2728

[33]JournaloftheChemicalSociety,1958,p.822,824

[34]ChemischeBerichte,1882,vol.15,p.2487    ChemischeBerichte,1885,vol.18,p.166

[35]JournalfurpraktischeChemie(Leipzig1954),1960,vol.11,p.239-248

[36]BerichtederBunsen-Gesellschaft,1992,vol.96,p.50-61

[37]JournalofPhysicalChemistry,1995,vol.99,p.8190-8195

[38]EuropeanJournalofOrganicChemistry,1999,p.607-616

[39]JournaloftheChemicalSociety.PerkintransactionsI,1999,p.2421-2423

[40]SyntheticCommunications,2007,vol.37,p.149-156

[41]Tetrahedron,2007,vol.63,p.6764-6773

[42]Patent:EP1589016,2005,A1.Locationinpatent:Page/Pagecolumn25

[43]TetrahedronLetters,2008,vol.49,p.6579-6584

[44]JournalofOrganicChemistry,2011,vol.76,p.1883-1886

[45]TetrahedronLetters,2013,vol.54,p.1428-1431

[46]ChemMedChem,2014,vol.9,p.177-188

[47]Chirality,2014,vol.26,p.272-278

[48]ChemicalCommunications,2015,vol.51,p.4028-4031

[49]ChemicalCommunications,2015,vol.51,p.12212-12215

[50]GreenChemistry,2015,vol.17,p.5009-5018

[51]GreenChemistry,2016,vol.18,p.2029-2036

[52]JournalofCatalysis,2017,vol.346,p.170-179

[53]GreenChemistry,2016,vol.18,p.6545-6555

[54]Patent:CN109020792,2018,A.Locationinpatent:Page/Pagecolumn5-7

[55]GreenChemistry,2019,vol.21,p.1974-1981

[56]MolecularDiversity,2019

[57]GreenChemistry,2019,vol.21,p.6707-6716

[58]JournaloftheAmericanChemicalSociety,2020,vol.142,p.4037-4050

[1]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[2]RSCAdvances,2016,vol.6,p.104742-104753

[3]ChemSusChem,2020,vol.13,p.1740-1745

[4]ChemCatChem,2015,vol.7,p.401-404

[5]GreenChemistry,2016,vol.18,p.2029-2036

[6]ACSCatalysis,2016,vol.6,p.6086-6090

[7]ChemicalCommunications,2019,vol.55,p.14143-14146

[8]TetrahedronLetters,2016,vol.57,p.3024-3028

[9]CanadianJournalofChemistry,1995,vol.73,p.2079-2085

[10]AngewandteChemie-InternationalEdition,2013,vol.52,p.12674-12678    Angew.Chem.,2013,vol.125,p.12906-12910

[11]InorganicChemistry,2014,vol.53,p.11377-11387

[12]GreenChemistry,2015,vol.17,p.5009-5018

[13]ACSCatalysis,2017,vol.7,p.4571-4580

[14]ACSCatalysis,2017,vol.7,p.3419-3429

[15]ChemCatChem,2019,vol.11,p.3786-3790

[16]GreenChemistry,2019,vol.21,p.2005-2014

[17]ACSCatalysis,2019,vol.9,p.11341-11349

[18]ACSCatalysis,2019,vol.9,p.11341-11349

[19]GreenChemistry,2020,vol.22,p.248-255

[1]OrganicLetters,2003,vol.5,p.4645-4648

Literature

Title: Effects of the antimycobacterial compound 2-phenoxy-1-phenylethanone on rat hepatocytes and formation of metabolites.

Journal: Pharmaceutical biology 20121001

Title: Antimycobacterial activity of 2-phenoxy-1-phenylethanone, a synthetic analogue of neolignan, entrapped in polymeric microparticles.

Journal: Drug development and industrial pharmacy 20120301

Title: Structure activity relationship, acute toxicity and cytotoxicity of antimycobacterial neolignan analogues.

Journal: The Journal of pharmacy and pharmacology 20110701

Title: Structure-activity relationship of antileishmanials neolignan analogues.

Journal: Bioorganic & medicinal chemistry 20071201

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

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SDS
Tags:721-04-0 Molecular Formula|721-04-0 MDL|721-04-0 SMILES|721-04-0 2-Phenoxyacetophenone
Catalog No.: AA00FE6I
721-04-0,MFCD00156689
721-04-0 | 2-Phenoxyacetophenone
Pack Size: 250mg
Purity: 98%
in stock
$32.00 $23.00
Pack Size: 1g
Purity: 98%
in stock
$102.00 $72.00
Pack Size: 5g
Purity: 98%
in stock
$296.00 $207.00
Quantity
- +
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Technical Information
Catalog Number: AA00FE6I
Chemical Name: 2-Phenoxyacetophenone
CAS Number: 721-04-0
Molecular Formula: C14H12O2
Molecular Weight: 212.2439
MDL Number: MFCD00156689
SMILES: O=C(c1ccccc1)COc1ccccc1
NSC Number: 7586
Properties
Complexity: 213  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.7  
Downstream Synthesis Route
721-04-0    4249-72-3 

[1]Chemistry-AEuropeanJournal,2020,vol.26,p.3641-3646

[2]JournaloftheAmericanChemicalSociety,2020,vol.142,p.4037-4050

[3]GreenChemistry,2016,vol.18,p.6229-6235

[4]DaltonTransactions,2017,vol.46,p.11884-11889

[5]GreenChemistry,2019,vol.21,p.2005-2014

[6]CatalysisToday,2016,vol.269,p.40-47

[7]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[8]ChemicalCommunications,2015,vol.51,p.4028-4031

[9]ACSCatalysis,2016,vol.6,p.1316-1328

[10]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12554-12555

[11]TetrahedronLetters,2010,vol.51,p.6418-6421

[12]ChemicalCommunications,2019,vol.55,p.13144-13147

[13]GreenChemistry,2020,vol.22,p.248-255

[14]Patent:US2016/52949,2016,A1.Locationinpatent:Paragraph0101

[15]GreenChemistry,2014,vol.16,p.2432-2437

[16]JournaloftheAmericanChemicalSociety,1958,vol.80,p.202

[17]JournaloftheChemicalSociety,1960,p.3521-3527

[18]JournaloftheChemicalSociety.PerkintransactionsII,1978,p.1135-1144

[19]ZeitschriftfurPhysikalischeChemie(Leipzig),1990,vol.271,p.927-930

[20]JournalofOrganicChemistry,2006,vol.71,p.7035-7044

[21]JournalofOrganicChemistry,2002,vol.67,p.7937-7945

[22]Tetrahedron,2008,vol.64,p.3867-3876

[23]JournalofOrganicChemistry,2011,vol.76,p.1883-1886

[24]ChemicalCommunications,2015,vol.51,p.12212-12215

[25]GreenChemistry,2015,vol.17,p.5009-5018

[26]GreenChemistry,2016,vol.18,p.2029-2036

[27]GreenChemistry,2016,vol.18,p.6545-6555

[28]GreenChemistry,2019,vol.21,p.1974-1981

[29]GreenChemistry,2019,vol.21,p.6707-6716

3598-14-9   
phenylmagnesiumbromide 
  721-04-0 

[1]JournaloftheAmericanChemicalSociety,1938,vol.60,p.1148,1150

70-11-1    108-95-2    721-04-0 

[1]GreenChemistry,2016,vol.18,p.6229-6235

[2]GreenChemistry,2017,vol.19,p.4538-4543

[3]DaltonTransactions,2017,vol.46,p.11884-11889

[4]GreenChemistry,2019,vol.21,p.2005-2014

[5]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12554-12555

[6]ChemicalCommunications,2019,vol.55,p.13144-13147

[7]SyntheticCommunications,1996,vol.26,p.301-305

[8]Chemistry-AEuropeanJournal,2020,vol.26,p.10402-10405

[9]JournalofOrganicChemistry,2014,vol.79,p.6153-6163

[10]ACSCatalysis,2019,vol.9,p.11341-11349

[11]SyntheticCommunications,2009,vol.39,p.4079-4087

[12]GreenChemistry,2017,vol.19,p.702-706

[13]BioorganicandMedicinalChemistry,1998,vol.6,p.825-832

[14]GreenChemistry,2013,vol.15,p.768-774

[15]ACSCatalysis,2016,vol.6,p.1316-1328

[16]Patent:US2016/52949,2016,A1.Locationinpatent:Paragraph0100

[17]GreenChemistry,2020,vol.22,p.248-255

[18]BioorganicandMedicinalChemistryLetters,1998,vol.8,p.2773-2776

[19]CatalysisToday,2016,vol.269,p.40-47

[20]OrganicLetters,2020,vol.22,p.6055-6060

[21]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[22]TetrahedronLetters,2016,vol.57,p.3024-3028

[23]BioorganicandMedicinalChemistry,2007,vol.15,p.7337-7343

[24]Tetrahedron,1999,vol.55,p.12699-12710

[25]Patent:US6392089,2002,B1.Locationinpatent:Pagecolumn26

[26]TetrahedronLetters,2010,vol.51,p.6418-6421

[27]Chemistry-AEuropeanJournal,2020,vol.26,p.3641-3646

[28]ChemicalBiologyandDrugDesign,2012,vol.80,p.591-597

[29]GreenChemistry,2014,vol.16,p.2432-2437

[30]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1999,vol.38,p.1108-1110

[31]Tetrahedron,2008,vol.64,p.3867-3876

[32]JournalofOrganicChemistry,2005,vol.70,p.2720-2728

[33]JournaloftheChemicalSociety,1958,p.822,824

[34]ChemischeBerichte,1882,vol.15,p.2487    ChemischeBerichte,1885,vol.18,p.166

[35]JournalfurpraktischeChemie(Leipzig1954),1960,vol.11,p.239-248

[36]BerichtederBunsen-Gesellschaft,1992,vol.96,p.50-61

[37]JournalofPhysicalChemistry,1995,vol.99,p.8190-8195

[38]EuropeanJournalofOrganicChemistry,1999,p.607-616

[39]JournaloftheChemicalSociety.PerkintransactionsI,1999,p.2421-2423

[40]SyntheticCommunications,2007,vol.37,p.149-156

[41]Tetrahedron,2007,vol.63,p.6764-6773

[42]Patent:EP1589016,2005,A1.Locationinpatent:Page/Pagecolumn25

[43]TetrahedronLetters,2008,vol.49,p.6579-6584

[44]JournalofOrganicChemistry,2011,vol.76,p.1883-1886

[45]TetrahedronLetters,2013,vol.54,p.1428-1431

[46]ChemMedChem,2014,vol.9,p.177-188

[47]Chirality,2014,vol.26,p.272-278

[48]ChemicalCommunications,2015,vol.51,p.4028-4031

[49]ChemicalCommunications,2015,vol.51,p.12212-12215

[50]GreenChemistry,2015,vol.17,p.5009-5018

[51]GreenChemistry,2016,vol.18,p.2029-2036

[52]JournalofCatalysis,2017,vol.346,p.170-179

[53]GreenChemistry,2016,vol.18,p.6545-6555

[54]Patent:CN109020792,2018,A.Locationinpatent:Page/Pagecolumn5-7

[55]GreenChemistry,2019,vol.21,p.1974-1981

[56]MolecularDiversity,2019

[57]GreenChemistry,2019,vol.21,p.6707-6716

[58]JournaloftheAmericanChemicalSociety,2020,vol.142,p.4037-4050

4249-72-3    721-04-0 

[1]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[2]RSCAdvances,2016,vol.6,p.104742-104753

[3]ChemSusChem,2020,vol.13,p.1740-1745

[4]ChemCatChem,2015,vol.7,p.401-404

[5]GreenChemistry,2016,vol.18,p.2029-2036

[6]ACSCatalysis,2016,vol.6,p.6086-6090

[7]ChemicalCommunications,2019,vol.55,p.14143-14146

[8]TetrahedronLetters,2016,vol.57,p.3024-3028

[9]CanadianJournalofChemistry,1995,vol.73,p.2079-2085

[10]AngewandteChemie-InternationalEdition,2013,vol.52,p.12674-12678    Angew.Chem.,2013,vol.125,p.12906-12910

[11]InorganicChemistry,2014,vol.53,p.11377-11387

[12]GreenChemistry,2015,vol.17,p.5009-5018

[13]ACSCatalysis,2017,vol.7,p.4571-4580

[14]ACSCatalysis,2017,vol.7,p.3419-3429

[15]ChemCatChem,2019,vol.11,p.3786-3790

[16]GreenChemistry,2019,vol.21,p.2005-2014

[17]ACSCatalysis,2019,vol.9,p.11341-11349

[18]ACSCatalysis,2019,vol.9,p.11341-11349

[19]GreenChemistry,2020,vol.22,p.248-255

3598-16-1    23665-09-0    721-04-0 

[1]OrganicLetters,2003,vol.5,p.4645-4648

Literature fold

Title: Effects of the antimycobacterial compound 2-phenoxy-1-phenylethanone on rat hepatocytes and formation of metabolites.

Journal: Pharmaceutical biology20121001

Title: Antimycobacterial activity of 2-phenoxy-1-phenylethanone, a synthetic analogue of neolignan, entrapped in polymeric microparticles.

Journal: Drug development and industrial pharmacy20120301

Title: Structure activity relationship, acute toxicity and cytotoxicity of antimycobacterial neolignan analogues.

Journal: The Journal of pharmacy and pharmacology20110701

Title: Structure-activity relationship of antileishmanials neolignan analogues.

Journal: Bioorganic & medicinal chemistry20071201

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology20060501

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