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Home Iodos 13329-40-3
13329-40-3,MFCD00045320
Catalog No.:AA0014H0

13329-40-3 | 4'-Iodoacetophenone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$6.00   $4.00
- +
10g
98%
in stock  
$8.00   $6.00
- +
25g
98%
in stock  
$16.00   $11.00
- +
100g
98%
in stock  
$44.00   $31.00
- +
500g
98%
in stock  
$217.00   $152.00
- +
  • 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:
AA0014H0
Chemical Name:
4'-Iodoacetophenone
CAS Number:
13329-40-3
Molecular Formula:
C8H7IO
Molecular Weight:
246.0451
MDL Number:
MFCD00045320
SMILES:
CC(=O)c1ccc(cc1)I
NSC Number:
97396
Properties
Properties
 
BP:
279.9 °C at 760 mmHg  
Form:
Solid  
MP:
82-84 °C  
Stability:
Light Sensitive  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
125  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.4  

Upstream Synthesis Route

[1]Patent:WO2005/107762,2005,A2,.Locationinpatent:Page/Pagecolumn265-266

[2]Patent:WO2007/56056,2007,A2,.Locationinpatent:Page/Pagecolumn60;69

[3]EuropeanJournalofMedicinalChemistry,2012,vol.53,p.246-253

[4]Patent:US2005/101602,2005,A1,.Locationinpatent:Page/Pagecolumn45

[5]Patent:US2005/159597,2005,A1,.Locationinpatent:Page/Pagecolumn30-31

[6]JournalofOrganicChemistry,2013,vol.78,#14,p.7312-7317

[7]JournalofOrganicChemistry,2007,vol.72,#8,p.2794-2802

[8]Patent:WO2013/59281,2013,A2,.Locationinpatent:Page/Pagecolumn33

[9]JournalofOrganicChemistry,2011,vol.76,#3,p.749-759

[10]BioorganicandMedicinalChemistryLetters,2011,vol.21,#10,p.2966-2968

[11]Patent:WO2005/41899,2005,A2,.Locationinpatent:Page/Pagecolumn128

[12]EuropeanJournalofOrganicChemistry,2013,#8,p.1551-1557

[13]Patent:WO2005/41899,2005,A2,.Locationinpatent:Page/Pagecolumn128

[14]BioorganicandMedicinalChemistryLetters,2005,vol.15,#15,p.3568-3572

[15]Patent:US2004/6108,2004,A1,.Locationinpatent:Page5;6

[16]Patent:US2010/249190,2010,A1,.Locationinpatent:Page/Pagecolumn80

[17]AustralianJournalofChemistry,1997,vol.50,#1,p.61-67

[18]Patent:CN107629023,2018,A,.Locationinpatent:Paragraph0190;0193;0194;0195

[19]Patent:CN107629022,2018,A,.Locationinpatent:Paragraph0304;0305;0306;0307

[20]AdvancedSynthesisandCatalysis,2018,vol.360,#3,p.568-574

[21]JournaloftheAmericanChemicalSociety,1920,vol.42,p.1049

[22]Patent:EP1582516,2005,A1,.Locationinpatent:Page/Pagecolumn83

[23]Patent:WO2007/56143,2007,A2,.Locationinpatent:Page/Pagecolumn58

[24]Patent:US2012/115898,2012,A1,.Locationinpatent:Page/Pagecolumn8

[25]JournalofMedicinalChemistry,2017,vol.60,#4,p.1591-1597

[26]OrganicLetters,2017,vol.19,#8,p.1994-1997

[27]OrganicLetters,2017,vol.19,#11,p.2877-2880

[28]EuropeanJournalofMedicinalChemistry,2018,vol.144,p.179-200

[29]OrganicLetters,2018,vol.20,#8,p.2257-2260

[1]ChemMedChem,2010,vol.5,#9,p.1541-1555

[1]JournaloftheAmericanChemicalSociety,1920,vol.42,p.1049

[1]JournalofOrganicChemistry,2008,vol.73,#9,p.3604-3607

[1]Synlett,2017,vol.28,#20,p.2833-2838

Downstream Synthesis Route

[1]Patent:WO2005/107762,2005,A2.Locationinpatent:Page/Pagecolumn265-266

[2]Patent:WO2007/56056,2007,A2.Locationinpatent:Page/Pagecolumn60;69

[3]EuropeanJournalofMedicinalChemistry,2012,vol.53,p.246-253

[4]Patent:US2005/101602,2005,A1.Locationinpatent:Page/Pagecolumn45

[5]Patent:US2005/159597,2005,A1.Locationinpatent:Page/Pagecolumn30-31

[6]JournalofOrganicChemistry,2013,vol.78,p.7312-7317

[7]JournalofOrganicChemistry,2007,vol.72,p.2794-2802

[8]Patent:WO2013/59281,2013,A2.Locationinpatent:Page/Pagecolumn33

[9]JournalofOrganicChemistry,2011,vol.76,p.749-759

[10]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.2966-2968

[11]EuropeanJournalofOrganicChemistry,2013,p.1551-1557

[12]Patent:WO2005/41899,2005,A2.Locationinpatent:Page/Pagecolumn128

[13]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.3568-3572

[14]Patent:US2004/6108,2004,A1.Locationinpatent:Page5;6

[15]Patent:US2010/249190,2010,A1.Locationinpatent:Page/Pagecolumn80

[16]AustralianJournalofChemistry,1997,vol.50,p.61-67

[17]Patent:CN107629023,2018,A.Locationinpatent:Paragraph0190;0193;0194;0195

[18]Patent:CN107629022,2018,A.Locationinpatent:Paragraph0304;0305;0306;0307

[19]AdvancedSynthesisandCatalysis,2018,vol.360,p.568-574

[20]JournaloftheAmericanChemicalSociety,1920,vol.42,p.1049

[21]Patent:EP1582516,2005,A1.Locationinpatent:Page/Pagecolumn83

[22]Patent:WO2007/56143,2007,A2.Locationinpatent:Page/Pagecolumn58

[23]Patent:US2012/115898,2012,A1.Locationinpatent:Page/Pagecolumn8

[24]JournalofMedicinalChemistry,2017,vol.60,p.1591-1597

[25]OrganicLetters,2017,vol.19,p.1994-1997

[26]OrganicLetters,2017,vol.19,p.2877-2880

[27]EuropeanJournalofMedicinalChemistry,2018,vol.144,p.179-200

[28]OrganicLetters,2018,vol.20,p.2257-2260

[29]MolecularDiversity,2018,p.1-15

[1]OrganicandBiomolecularChemistry,2007,vol.5,p.65-68

[2]Synlett,2007,p.2006-2010

[3]RSCAdvances,2015,vol.5,p.94776-94785

[4]TetrahedronLetters,1991,vol.32,p.4733-4736

[5]AppliedOrganometallicChemistry,2019,vol.33

[6]JournalofMolecularCatalysisA:Chemical,2015,vol.398,p.164-169

[7]Tetrahedron,2008,vol.64,p.9581-9584

[8]ACSCatalysis,2013,vol.3,p.287-293

[9]JournalofOrganicChemistry,1991,vol.56,p.4320-4322

[10]OrganicProcessResearchandDevelopment,2009,vol.13,p.634-637

[11]Organicprocessresearchanddevelopment,2011,vol.15,p.717-720

[12]ChemicalCommunications,2018,vol.54,p.8100-8103

[1]JournalofOrganicChemistry,1997,vol.62,p.6458-6459

[2]JournalofOrganicChemistry,2000,vol.65,p.164-168

[3]Patent:US7034045,2006,B1.Locationinpatent:Page/Pagecolumn76

[4]Patent:US7034045,2006,B1.Locationinpatent:Page/Pagecolumn85

1885-38-7    13329-40-3    787-69-9   
(Z)-3-(4-acetylphenyl)-3-phenyl-2-propenenitrile 
 
(E)-3-(4-acetylphenyl)-3-phenyl-2-propenenitrile 

[1]Synlett,1997,vol.1997,p.1157-1158

[1]JournaloftheAmericanChemicalSociety,1920,vol.42,p.1049

Literature

Title: Bioconversion of iodoacetophenones by marine fungi.

Journal: Marine biotechnology (New York, N.Y.) 20120801

Title: Effects of a fluorescent Myosin light chain phosphatase inhibitor on prostate cancer cells.

Journal: Frontiers in oncology 20110101

Title: Synthesis and biological evaluation of NAS-21 and NAS-91 analogues as potential inhibitors of the mycobacterial FAS-II dehydratase enzyme Rv0636.

Journal: Microbiology (Reading, England) 20080701

Title: p-Chloro-, p-bromo- and two polymorphs of p-iodoacetophenone.

Journal: Acta crystallographica. Section C, Crystal structure communications 20040801

Title: 13C NMR study of halogen bonding of haloarenes: measurements of solvent effects and theoretical analysis.

Journal: Journal of the American Chemical Society 20040407

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