106263-50-7

Basic information

• Product Name: 4-(2-CHLOROPHENYL)-4-OXOBUTYRIC ACID
• Synonyms: 4-(2-CHLOROPHENYL)-4-OXOBUTYRIC ACID;4-(2-Chlorophenyl)-4-oxobutanoic acid
• CAS NO: 106263-50-7
• Molecular Formula: C₁₀H₉ClO₃
• Molecular Weight: 212.63
• Mol File: 106263-50-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 363.7°C at 760 mmHg
• Flash Point: 173.7°C
• Appearance: /
• Density: 1.324g/cm³
• Vapor Pressure: 6.31E-06mmHg at 25°C
• Refractive Index: 1.561
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-(2-CHLOROPHENYL)-4-OXOBUTYRIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-CHLOROPHENYL)-4-OXOBUTYRIC ACID(106263-50-7)
• EPA Substance Registry System: 4-(2-CHLOROPHENYL)-4-OXOBUTYRIC ACID(106263-50-7)

Safety Data

• Hazardous Substances Data: 106263-50-7(Hazardous Substances Data)

Usage

General Description

4-(2-chlorophenyl)-4-oxobutyric acid is a chemical compound with the molecular formula C10H9ClO3. It is a synthetic organic compound that is used in research and in the production of pharmaceuticals. 4-(2-CHLOROPHENYL)-4-OXOBUTYRIC ACID is a derivative of butyric acid, which is a carboxylic acid that is found in many plants and animal fats. The addition of a 2-chlorophenyl group to butyric acid creates a new compound with potentially different properties and uses. Studies have shown that 4-(2-chlorophenyl)-4-oxobutyric acid may have potential therapeutic properties, making it an interesting target for further research in the pharmaceutical industry.

InChI:InChI=1/C10H9ClO3/c11-8-4-2-1-3-7(8)9(12)5-6-10(13)14/h1-4H,5-6H2,(H,13,14)

Upstream product

• 108-30-5 succinic acid anhydride 
• 694-80-4 2-bromo-1-chlorobenzene 
• 108-90-7 chlorobenzene 
• 106-46-7 para-dichlorobenzene 

Downstream Products

• 106263-52-9 4,5-dihydro-2-(2-nitrophenyl)-6-<2-(chlorophenyl)>-3(2H)-pyridazinone 
• 106263-38-1 6-(2-chlorophenyl)-2-(2-nitrophenyl)-3(2H)-pyridazinone 
• 106263-49-4 2-(2-chlorophenyl)pyridazino<1,6-a>benzimidazole 

Relevant articles and documents

Asymmetric hydrogenation reaction γ - or δ - ketonato compound (by machine translation)

The invention relates to the field, of organic chemistry, specifically γ - or δ - keto acid compound asymmetric hydrogenation reaction, reaction formula as follows : Wherein R is H,C. 1 - C6 An alkyl or halogen, is R 1 - 5 in number of substituents . wherein n is 1 or 2;Cat. is a chiral spiro pyrimidyl phosphine ligand iridium complex . and γ - or δ - keto acid compound is subjected to an internal esterification reaction to further prepare a lactone compound. (by machine translation)

Organic qualitative analysis. IV. Identification of carboxylic acids by S-(p-nitrobenzyl)- and S-(2,4-dinitrobenzyl)-thiuronium chloride.

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