2706-75-4

Basic information

• Product Name: SODIUM GLYOXYLATE
• Synonyms: SODIUM GLYOXYLATE;oxo-aceticacisodiumsalt;GLYOXYLIC ACID SODIUM SALT;glyoxylic acid sodium monohydrate;MONOSODIUMGLYOXYLATE;GLYOXLIC ACID SODIUM SALT;Glyoxylic acid monohydrate sodium salt, Oxoethanoic acid sodium salt;2-Oxoacetic acid sodium salt
• CAS NO: 2706-75-4
• Molecular Formula: C₂HO₃*Na
• Molecular Weight: 96.02
• EINECS: 220-298-8
• Mol File: 2706-75-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 224.6 °C at 760 mmHg
• Flash Point: 103.9 °C
• Appearance: /
• Density: 1.384g/cm³
• Vapor Pressure: 0.0331mmHg at 25°C
• Refractive Index: 1.403
• Storage Temp.: −20°C
• CAS DataBase Reference: SODIUM GLYOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: SODIUM GLYOXYLATE(2706-75-4)
• EPA Substance Registry System: SODIUM GLYOXYLATE(2706-75-4)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• RTECS: MD4725000
• Hazardous Substances Data: 2706-75-4(Hazardous Substances Data)

Usage

Definition

ChEBI: An organic sodium salt that is the monosodium salt of glyoxylic acid.

InChI:InChI=1/C2H2O3/c3-1-2(4)5/h1H,(H,4,5)

Upstream product

• 1310-73-2 sodium hydroxide 
• 298-12-4 Glyoxilic acid 

Downstream Products

• 35045-66-0 4-(2,4-dimethoxy-phenyl)-2-morpholin-4-yl-4-oxo-butyric acid 
• 21813-64-9 2-morpholin-4-yl-4-(4-nitro-phenyl)-4-oxo-butyric acid 
• 122-87-2 N-(hydroxyphenyl)glycine 
• 34911-59-6 ((E)-2-oxo-cyclohexyliden)-acetic acid 
• 57470-04-9 N-(4-Chloro-phenyl)-N-hydroxy-formamide 
• 73747-07-6 N-(4-Tolyl)formohydroxamsaeure 
• 1186-90-9 erythro-β-hydroxy-DL-aspartic acid 
• 4294-45-5 DL-threo-β-hydroxyaspartic acid 
• 35045-63-7 4-(3-methoxy-phenyl)-2-morpholin-4-yl-4-oxo-butyric acid 
• 35045-68-2 (5-acetyl-2-hydroxy-phenyl)-morpholin-4-yl-acetic acid 
• 35046-31-2 2-morpholin-4-yl-4-(3-nitro-phenyl)-4-oxo-butyric acid 
• 21813-65-0 4-(4-methoxy-phenyl)-2-morpholin-4-yl-4-oxo-butyric acid 
• 35046-27-6 2-(N-Morpholino)-3-p-brombenzoyl-propionsaeure 
• 21813-63-8 4-(4-Chlorphenyl)-2-morpholino-4-oxo-butansaeure 

Relevant articles and documents

PROCESS FOR REMOVING HYDROGEN CYANIDE FROM ETHANEDINITRILE

Process for removing hydrogen cyanide from ethanedinitrile by contacting hydrogen cyanide-containing ethanedinitrile with an organic reagent under formation of a covalent bond.

BISULFITE PURIFICATION OF AN ALPHA-KETO AMIDE

A process for purifying the alpha-keto amide is (1R,5S)-N-[3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl]-3-[2(S)-[[[(1,1-dimethylethyl)amino]carbonyl]-amino]-3,3-dimethyl-1-oxobutyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexan-2(S)-carboxamide via a bisulfite adduct is disclosed.

Asymmetric hydrogenation process

The present invention provides an asymmetric hydrogenation process for the preparation of chiral cycloalkanoindole DP receptor antagonists in high enantiomeric excess.