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7163-50-0,MFCD00961859
Catalog No.:AA005RCO

7163-50-0 | (4-Methylphenyl)(oxo)acetic acid

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100mg
tech
in stock  
$72.00   $50.00
- +
1g
96%
in stock  
$112.00   $78.00
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5g
96%
in stock  
$311.00   $218.00
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10g
96%
in stock  
$477.00   $334.00
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25g
96%
in stock  
$809.00   $567.00
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100g
96%
in stock  
$2,007.00   $1,405.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA005RCO
Chemical Name:
(4-Methylphenyl)(oxo)acetic acid
CAS Number:
7163-50-0
Molecular Formula:
C9H8O3
Molecular Weight:
164.1580
MDL Number:
MFCD00961859
SMILES:
O=C(c1ccc(cc1)C)C(=O)O
Properties
Properties
 
BP:
290.6 °C at 760 mmHg  
Form:
Solid  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
190  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
1.7  

Downstream Synthesis Route

[1]BioorganicandMedicinalChemistry,1997,vol.5,p.1555-1567

[2]JournaloftheAmericanChemicalSociety,2019,vol.141,p.16237-16242

[3]JournalofOrganicChemistryUSSR(EnglishTranslation),1966,vol.2,p.14-15    ZhurnalOrganicheskoiKhimii,1966,vol.2,p.17-19

[4]JournalofMedicinalChemistry,1981,vol.24,p.399-404

[5]JournaloftheAmericanChemicalSociety,1995,vol.117,p.3999-4013

[6]Patent:EP1486483,2004,A1.Locationinpatent:Page29

[7]Patent:EP1541557,2005,A1.Locationinpatent:Page/Pagecolumn49

[8]CatalysisToday,2012,vol.198,p.345-352

[9]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2013,vol.52,p.818-823

[10]ChemicalCommunications,2014,vol.50,p.4489-4491

[11]BioorganicandMedicinalChemistryLetters,2014,vol.24,p.1958-1962

[12]BeilsteinJournalofOrganicChemistry,2018,vol.14,p.1215-1221

[13]Chemistry-AEuropeanJournal,2018,vol.24,p.8114-8125

[14]OrganicLetters,2019,vol.21,p.7119-7123

[15]OrganicLetters,2020,vol.22,p.4974-4978

[16]TetrahedronLetters,2020,vol.61

2216-52-6    7163-50-0   
(+)-<(1S,2S,5R)-2-Isopropyl-5-methylcyclohexyl>-4-methylphenylglyoxylat 

[1]Pelzer,Ralf;Scharf,Hans-Dieter;Buschmann,Helmut;Runsink,Jan[ChemischeBerichte,1989,vol.122,p.1187-1192]

[1]TetrahedronLetters,2013,vol.54,p.5387-5390

[2]JournalofOrganicChemistry,1980,vol.45,p.2976-2984

[3]ChemicalBiologyandDrugDesign,2016,vol.87,p.112-120

[1]AdvancedSynthesisandCatalysis,2013,vol.355,p.1517-1522

[1]Mahaveer;Kulkarni;Radakrishna;Chandrashekar;Achaiah[IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2013,vol.52,#6,p.818-823]

Literature

Title: Integration of newly isolated biocatalyst and resin-based in situ product removal technique for the asymmetric synthesis of (R)-methyl mandelate.

Journal: Bioprocess and biosystems engineering 20100901

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