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7-Aminodesacetoxycephalosporanic acid_Molecular_structure_CAS_22252-43-3)
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7-Aminodesacetoxycephalosporanic acid

Catalog No. A8398 Name Sigma Aldrich
CAS Number 22252-43-3 Website http://www.sigmaaldrich.com
M. F. C8H10N2O3S Telephone 1-800-521-8956
M. W. 214.2416 Fax
Purity Email
Storage Chembase ID: 104099

SYNONYMS

IUPAC name
(6R,7R)-7-amino-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
IUPAC Traditional name
(6R,7R)-7-amino-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Synonyms
7-ADCA

DATABASE IDS

MDL Number MFCD09750368
EC Number 244-870-1
PubChem SID 24891339
CAS Number 22252-43-3

PROPERTIES

Empirical Formula (Hill Notation) C8H10N2O3S
Solubility Do you have solubility information on this product that you would like to share?
GHS Pictograms GHS08
GHS Signal Word Danger
GHS Hazard statements H317-H334
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS Precautionary statements P261-P280-P342 + P311
Risk Statements 42/43
Safety Statements 36
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Application
Do you have application information on this product that you would like to share?
7-Aminodesacetoxycephalosporanic acid is used in the synthesis of cephalosporins and for bioconversion studies 1.
7-Aminodesacetoxycephalosporanic acid is used in the synthesis of cephalosporins.
Biochem/physiol Actions
7-ADCA is produced from penicillin G made by Penicillium chrysogenum involving several polluting chemical steps followed by enzymatic deacylation using penicillin acylase 2.
Description (简体中文)
Application
Do you have application information on this product that you would like to share?
7-Aminodesacetoxycephalosporanic acid is used in the synthesis of cephalosporins and for bioconversion studies 1.
7-Aminodesacetoxycephalosporanic acid is used in the synthesis of cephalosporins.
Biochem/physiol Actions
7-ADCA is produced from penicillin G made by Penicillium chrysogenum involving several polluting chemical steps followed by enzymatic deacylation using penicillin acylase 2.

REFERENCES