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

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

• 6000-60-8 phenylhydrazonoacetic acid 
• 55-10-7 4-hydroxy-3-methoxy-mandelic acid 
• 37520-05-1 2-hydroxy-acetoacetic acid 
• 918-44-5 alpha-acetyllactic acid 
• 122-87-2 N-(hydroxyphenyl)glycine 
• 31335-69-0 N-hydroxy-N-formylaniline 
• 62-76-0 sodium oxalate 
• 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 

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.

CROSSLINKING AGENT, CROSSLINKED POLYMER, AND USES THEREOF

There is provided a novel crosslinking agent for use in crosslinked polymer fabrication, specifically a crosslinking agent containing at least one compound selected from glyoxylate and a glyoxylic acid ester derivative represented by the following general formula (1): wherein R1 and R2 each independently represents an alkyl group having 1 to 10 carbon atoms and R3 represents a hydrogen atom or an alkyl group having 1 to 10 carbon atoms.

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.

Asymmetrically substituted phosphinic acids

The invention relates to asymmetrically substituted phosphinic acids of the formula (I) [in-line-formulae]R1R2C(OH)—P(═O)(OX)—C(OH)R3R4 ??(I)[/in-line-formulae] in which X is hydrogenR1, R2, R3, and R4 are identical or different and are hydrogen, alkyl, alkenyl, alkynyl, aralkyl, aryl and/or alkaryl,with the proviso that the respective R1R2C(OH)— and —C(OH)R3R4 groups are always different, to a process for their preparation, and to their use.

Asymmetric hydrogenation process

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

Process for preparing a hydroxyphenylglycine compound

Glyoxylic acid or a salt of glyoxylic, an ammonium salt of an organic or inorganic acid and a phenol compound of the formula: STR1 wherein n is an integer of one to three, are condensed together to prepare hydroxyphenylglycine compounds of the formula: STR2 wherein n is the same as defined above. The hydroxyphenylglycine compounds thus obtained are useful as intermediates in the synthesis of penicillins and cephalosporins.