43165-51-1

Basic information

• Product Name: sodium phenylglyoxylate
• Synonyms: sodium phenylglyoxylate;BENZOYLFORMIC ACID, SODIUM SALT;sodium benzoylformate;2-Phenylglyoxylic acid sodium salt;Oxophenylacetic acid sodium salt;α-Oxobenzeneacetic acid sodium salt;Benzeneacetic acid, a-oxo-, sodiuM salt
• CAS NO: 43165-51-1
• Molecular Formula: C₈H₅O₃*Na
• Molecular Weight: 172.11327
• EINECS: 256-125-8
• Mol File: 43165-51-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 258.6°C at 760 mmHg
• Flash Point: 124.4°C
• Appearance: /
• Vapor Pressure: 0.00697mmHg at 25°C
• CAS DataBase Reference: sodium phenylglyoxylate(CAS DataBase Reference)
• NIST Chemistry Reference: sodium phenylglyoxylate(43165-51-1)
• EPA Substance Registry System: sodium phenylglyoxylate(43165-51-1)

Safety Data

• Hazardous Substances Data: 43165-51-1(Hazardous Substances Data)

Usage

Description

Sodium phenylglyoxylate is a chemical compound composed of sodium and phenylglyoxylate, known for its stability, solubility in water, and low toxicity. It is commonly used in organic synthesis, pharmaceutical production, and as a key precursor in the preparation of various types of polymers.

Uses

Used in Organic Synthesis:
Sodium phenylglyoxylate is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of desired products.
Used in Pharmaceutical Production:
Sodium phenylglyoxylate is used as an intermediate in the production of pharmaceuticals, playing a crucial role in the synthesis of active ingredients for various medications.
Used in Polymer Preparation:
Sodium phenylglyoxylate is used as a key precursor in the preparation of different types of polymers, enabling the creation of materials with specific properties for diverse applications.
Used in Industrial Processes:
Sodium phenylglyoxylate is utilized in various industrial processes due to its versatility, stability, and water solubility, making it a valuable component in the development and manufacturing of numerous products.

InChI:InChI=1/C8H6O3.Na/c9-7(8(10)11)6-4-2-1-3-5-6;/h1-5H,(H,10,11);/q;+1/p-1

Upstream product

• 54385-47-6 (R)-Mandelsaeure, Natrium-Salz 
• 611-73-4 Benzoylformic acid 

Downstream Products

• 35147-13-8 Oxo-phenyl-acetic acid (S)-1-tert-butyl-pentyl ester 
• 25726-04-9 phenylglyoxylyl chloride 
• 611-71-2 (R)-Mandelic Acid 
• 85152-75-6 4-chlorobenzyl 2-oxo-2-phenylacetate 
• 41158-32-1 methyl 4-oxo-4-phenylbut-2-ynoate 
• 54966-47-1 4-oxo-4-phenyl-but-2-ynoic acid ethyl ester 
• 1087-09-8 1,4-diphenyl-but-2-yne-1,4-dione 
• 144823-67-6 methyl 3,4-dioxo-4-phenyl-2-triphenylphosphoranylidenebutanoate 
• 64875-44-1 1,4-diphenyl-3-triphenylphosporanylidenebutane-1,2,4-trione 
• 152126-77-7 ethyl 3,4-dioxo-4-phenyl-2-triphenylphosphoranylidenebutanoate 
• 162396-11-4 5,5-dimethyl-1-phenyl-3-triphenylphosphoranylidenehexane-1,2,4-trione 
• 724-92-5 N-cicloesil-α-ossofenilacetamide 
• 71835-48-8 acido (Z)-α-(4-nitrobenzilossicarbonilidrazono)fenilacetico 
• 131022-63-4 2-(p-methylphenyl)-5-phenyl-3,4-oxadiazin-6-one 

Relevant articles and documents

Catalytic O2activation with synthetic models of α-ketoglutarate dependent oxygenases

An iron complex bearing the facially capping tridentate 1,4,7-triazacyclononane ligand mimics structural and functional features of alpha-ketoglutarate (α-KG) dependent enzymes, and engages in enzyme-like catalytic O2 activation coupled to α-ketoacid decarboxylation, oxygenating sulfides. This system constitutes a rare case of non-enzymatic catalytic O2 activation, cycling between FeII and FeIV(O).