1074-12-0,MFCD00006959
Catalog No.:AA0035EE

1074-12-0 | Phenylglyoxal

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%(GC)
in stock  
$34.00   $24.00
- +
5g
95%
in stock  
$75.00   $53.00
- +
10g
95%
in stock  
$124.00   $87.00
- +
25g
95%
in stock  
$261.00   $183.00
- +
100g
95%
in stock  
$870.00 $609.00
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0035EE
Chemical Name:
Phenylglyoxal
CAS Number:
1074-12-0
Molecular Formula:
C8H6O2
Molecular Weight:
134.1320
MDL Number:
MFCD00006959
SMILES:
O=CC(=O)c1ccccc1
Properties
Properties
 
BP:
142°C at 760 mmHg  
Form:
Solid  
MP:
76 °C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
134  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.7  

Upstream Synthesis Route

[1]Patent:WO2009/112845,2009,A1,.Locationinpatent:Page/Pagecolumn140-141

[1]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[2]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[3]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[4]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[5]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[6]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[1]Patent:US2010/16303,2010,A1,.Locationinpatent:Page/Pagecolumn19

[2]Patent:WO2012/7006,2012,A1,.Locationinpatent:Page/Pagecolumn60

[3]Patent:WO2009/152825,2009,A1,.Locationinpatent:Page/Pagecolumn46

[1]JournalofHeterocyclicChemistry,1987,vol.24,p.441-451

[2]JournalofHeterocyclicChemistry,1981,vol.18,p.1651-1653

[3]TetrahedronLetters,2011,vol.52,#31,p.4036-4038

[4]Synthesis,2012,vol.44,#1,p.69-82

[5]Tetrahedron,2013,vol.69,#1,p.22-28

[6]TurkishJournalofChemistry,2015,vol.39,#2,p.244-254

[7]ResearchonChemicalIntermediates,2017,vol.43,#7,p.3925-3937

[8]AustralianJournalofChemistry,2015,vol.68,#10,p.1529-1534

[9]JournalofOrganicChemistry,2016,vol.81,#15,p.6402-6408

[1]OrganicLetters,2012,vol.14,#20,p.5378-5381,4

[2]OrganicLetters,2014,vol.16,#17,p.4582-4585

[3]JournalofOrganicChemistry,2015,vol.80,#11,p.5984-5991

[4]AdvancedSynthesisandCatalysis,2017,vol.359,#3,p.395-401

[5]OrganicLetters,2017,vol.19,#12,p.3319-3322

[6]JournalofOrganicChemistry,2017,vol.82,#24,p.13671-13677

[7]OrganicLetters,2018,vol.20,#3,p.688-691

[8]Tetrahedron,2018,vol.74,#32,p.4323-4330

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1949,vol.71,p.78,79,80

[1]ActaChemicaScandinavica(1947),1950,vol.4,p.892,893,897

[1]ChemistryofHeterocyclicCompounds,1978,vol.14,p.500-502    KhimiyaGeterotsiklicheskikhSoedinenii,1978,vol.14,p.613-615

[2]JournalofOrganicChemistry,1978,vol.43,p.341-343

[3]RussianChemicalBulletin,2018,vol.67,p.1078-1082    Izv.Akad.Nauk,Ser.Khim.,2018,p.1078-1082,5

88497-27-2    1074-12-0   
6-bromo-2-phenylimidazo<1,2-b>pyridazin-3(5H)-one 

[1]AustralianJournalofChemistry,1986,vol.39,p.1803-1809

[1]AustralianJournalofChemistry,1986,vol.39,p.1803-1809

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Tags:1074-12-0 Molecular Formula|1074-12-0 MDL|1074-12-0 SMILES|1074-12-0 Phenylglyoxal
Catalog No.: AA0035EE
1074-12-0,MFCD00006959
1074-12-0 | Phenylglyoxal
Pack Size: 1g
Purity: 98%(GC)
in stock
$34.00 $24.00
Pack Size: 5g
Purity: 95%
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$75.00 $53.00
Pack Size: 10g
Purity: 95%
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$124.00 $87.00
Pack Size: 25g
Purity: 95%
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$261.00 $183.00
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Purity: 95%
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Technical Information
Catalog Number: AA0035EE
Chemical Name: Phenylglyoxal
CAS Number: 1074-12-0
Molecular Formula: C8H6O2
Molecular Weight: 134.1320
MDL Number: MFCD00006959
SMILES: O=CC(=O)c1ccccc1
Properties
BP: 142°C at 760 mmHg  
Form: Solid  
MP: 76 °C  
Storage: Keep in dry area;2-8℃;  
Complexity: 134  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.7  
Upstream Synthesis Route
1074-12-0    107-15-3    5271-26-1 

[1]Patent:WO2009/112845,2009,A1,.Locationinpatent:Page/Pagecolumn140-141

1074-12-0    41270-62-6 

[1]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[2]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[3]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[4]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[5]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

[6]JournalofHeterocyclicChemistry,1982,vol.19,p.1061-1067

51673-84-8    1074-12-0    56248-10-3 

[1]Patent:US2010/16303,2010,A1,.Locationinpatent:Page/Pagecolumn19

[2]Patent:WO2012/7006,2012,A1,.Locationinpatent:Page/Pagecolumn60

[3]Patent:WO2009/152825,2009,A1,.Locationinpatent:Page/Pagecolumn46

1074-12-0    1075-06-5 

[1]JournalofHeterocyclicChemistry,1987,vol.24,p.441-451

[2]JournalofHeterocyclicChemistry,1981,vol.18,p.1651-1653

[3]TetrahedronLetters,2011,vol.52,#31,p.4036-4038

[4]Synthesis,2012,vol.44,#1,p.69-82

[5]Tetrahedron,2013,vol.69,#1,p.22-28

[6]TurkishJournalofChemistry,2015,vol.39,#2,p.244-254

[7]ResearchonChemicalIntermediates,2017,vol.43,#7,p.3925-3937

[8]AustralianJournalofChemistry,2015,vol.68,#10,p.1529-1534

[9]JournalofOrganicChemistry,2016,vol.81,#15,p.6402-6408

98-86-2    1074-12-0    1075-06-5 

[1]OrganicLetters,2012,vol.14,#20,p.5378-5381,4

[2]OrganicLetters,2014,vol.16,#17,p.4582-4585

[3]JournalofOrganicChemistry,2015,vol.80,#11,p.5984-5991

[4]AdvancedSynthesisandCatalysis,2017,vol.359,#3,p.395-401

[5]OrganicLetters,2017,vol.19,#12,p.3319-3322

[6]JournalofOrganicChemistry,2017,vol.82,#24,p.13671-13677

[7]OrganicLetters,2018,vol.20,#3,p.688-691

[8]Tetrahedron,2018,vol.74,#32,p.4323-4330

Downstream Synthesis Route
62009-47-6    1074-12-0    67602-11-3 

[1]JournaloftheAmericanChemicalSociety,1949,vol.71,p.78,79,80

1074-12-0    57-13-6    89-24-7    82264-50-4 

[1]ActaChemicaScandinavica(1947),1950,vol.4,p.892,893,897

1074-12-0    17220-38-1    64163-29-7 

[1]ChemistryofHeterocyclicCompounds,1978,vol.14,p.500-502    KhimiyaGeterotsiklicheskikhSoedinenii,1978,vol.14,p.613-615

[2]JournalofOrganicChemistry,1978,vol.43,p.341-343

[3]RussianChemicalBulletin,2018,vol.67,p.1078-1082    Izv.Akad.Nauk,Ser.Khim.,2018,p.1078-1082,5

88497-27-2    1074-12-0   
6-bromo-2-phenylimidazo<1,2-b>pyridazin-3(5H)-one 

[1]AustralianJournalofChemistry,1986,vol.39,p.1803-1809

66346-87-0    1074-12-0    108784-40-3 

[1]AustralianJournalofChemistry,1986,vol.39,p.1803-1809

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Journal: Therapie20020101

Title: [Characterization of urokinase type plasminogen activator modified by phenylglyoxal].

Journal: Bioorganicheskaia khimiia20020101

Title: Control of particle size by coagulation of novel condensation aerosols in reservoir chambers.

Journal: Journal of aerosol medicine : the official journal of the International Society for Aerosols in Medicine20020101

Title: Isolation and expression of a Bacillus cereus gene encoding benzil reductase.

Journal: Biotechnology and bioengineering20011220

Title: Increase in intrinsic anion conductance upon inhibition of the electroneutral Cl(-)/HCO(3)(-) exchanger: effect of CO(2)/HCO(3)(-).

Journal: Bioelectrochemistry (Amsterdam, Netherlands)20011101

Title: Protective effects of suprofen and its methyl ester against inactivation of rabbit kidney carbonyl reductase by phenylglyoxal.

Journal: Journal of enzyme inhibition20011101

Title: Regulation of catalytic activity of a multifunctional polyketide biosynthetic enzyme, 6-hydroxymellein synthase, by interaction between NADPH and phenylglyoxal-sensitive amino acid residue at the reaction center.

Journal: Biochimica et biophysica acta20010910

Title: Identification of functionally important amino-terminal arginines of Agrobacterium tumefaciens ADP-glucose pyrophosphorylase by alanine scanning mutagenesis.

Journal: Biochemistry20010828

Title: Functional residues on the enzyme active site of glyoxalase I from bovine brain.

Journal: Preparative biochemistry & biotechnology20010801

Title: Expression and characterization of recombinant rat Acyl-CoA synthetases 1, 4, and 5. Selective inhibition by triacsin C and thiazolidinediones.

Journal: The Journal of biological chemistry20010706

Title: Determination of anti-virus drug, ganciclovir, in human serum by HPLC with precolumn fluorescence derivatization using phenylglyoxal.

Journal: Analytical sciences : the international journal of the Japan Society for Analytical Chemistry20010701

Title: Inactivation of protein farnesyltransferase by active-site-targeted dicarbonyl compounds.

Journal: Archiv der Pharmazie20010601

Title: Diphenylamine-2-carboxylic acid (DPC), Usually an inhibitor of Cl- and non-selective cation channels, inhibits Cl-/HCO3- exchange and opens Cl- and cation conductances in rabbit gallbladder epithelium.

Journal: Pflugers Archiv : European journal of physiology20010601

Title: The production of reactive oxygen species by irradiated camphorquinone-related photosensitizers and their effect on cytotoxicity.

Journal: Archives of oral biology20010501

Title: Reduced enzymatic activity of glucokinase after affinity labeling: results from spectrophotometry and electrospray ionization mass spectrometry.

Journal: Journal of protein chemistry20010501

Title: Purification and characterization of the maize amyloplast stromal 112-kDa starch phosphorylase.

Journal: Archives of biochemistry and biophysics20010401

Title: Identification of the bile acid-binding site of the ileal lipid-binding protein by photoaffinity labeling, matrix-assisted laser desorption ionization-mass spectrometry, and NMR structure.

Journal: The Journal of biological chemistry20010309

Title: A stress-responsive glyoxalase I from the parasitic nematode Onchocerca volvulus.

Journal: The Biochemical journal20010201

Title: An essential role of active site arginine residue in iodide binding and histidine residue in electron transfer for iodide oxidation by horseradish peroxidase.

Journal: Molecular and cellular biochemistry20010201

Title: Crystal structure of the hydrated strontium salt of methotrexate: two independent molecules with different conformations.

Journal: Journal of medicinal chemistry20010118

Title: The effect of amino acid-modifying reagents on chloroplast protein import and the formation of early import intermediates.

Journal: Journal of experimental botany20010101

Title: Inhibitors of the Cl-/HCO3- exchanger activate an apical anion conductance with similar features in the epithelial cells of rabbit gallbladder: analysis in intact epithelium.

Journal: Pflugers Archiv : European journal of physiology20010101

Title: Inhibitors of the Cl-/HCO3- exchanger activate an anion channel with similar features in the epithelial cells of rabbit gallbladder: patch-clamp analysis.

Journal: Pflugers Archiv : European journal of physiology20010101

Title: Evidence for an essential arginine in the flavoprotein nitroalkane oxidase.

Journal: Journal of enzyme inhibition20010101

Title: Major differences exist in the function and tissue-specific expression of human aflatoxin B1 aldehyde reductase and the principal human aldo-keto reductase AKR1 family members.

Journal: The Biochemical journal19991015

Title: Role of basic amino acids in the interaction of bindin with sulfated fucans.

Journal: Biochemistry19881018

Title: Identification of an essential arginine residue in the beta subunit of the chloroplast ATPase.

Journal: The Journal of biological chemistry19850425

Title: Human liver prenyltransferase and its characterization.

Journal: Biochimica et biophysica acta19810915

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