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61-24-5

7-(5-amino-5-carboxyvaleramido)cephalosporanic acid

CAS: 61-24-5

Molecular Formula: C16H21N3O8S

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61-24-5 - Names and Identifiers

Name 7-(5-amino-5-carboxyvaleramido)cephalosporanic acid
Synonyms CAPHALOSPORIN C
Cefodizime impurity 16
Cephalosporins-intermediate II
7-(5-amino-5-carboxyvaleramido)cephalosporanic acid
7-(D-5-Amino-5-carboxyvaleramido)-3-(hydrox-ymethyl)-8-oxo-5-thia-1-azabicyclo[4,2,0]oct-2-ene-2-Carboxylic acid acetate
5-Thia-1-azabicyclo4.2.0oct-2-ene-2-carboxylic acid, 3-(acetyloxy)methyl-7-(5R)-5-amino-5-carboxy-1-oxopentylamino-8-oxo-, (6R,7R)-
CAS 61-24-5
EINECS 200-501-6

61-24-5 - Physico-chemical Properties

Molecular FormulaC16H21N3O8S
Molar Mass415.42
Density1.55±0.1 g/cm3(Predicted)
Boling Point814.7±65.0 °C(Predicted)
pKa2.49±0.24(Predicted)
Physical and Chemical PropertiesChemical properties Its sodium salt dihydrate is monoclinic crystal. Soluble in water, insoluble in ethanol and ether. When the aqueous solution is stable at pH 2.5-8.
UseUse of Staphylococcus aureus, Salmonella Typhi, Escherichia coli activity. However, due to low antibacterial activity, clinical not widely used. However, highly efficient derivatives can be obtained by modification, and are currently mainly used as intermediates for the preparation of 7-aminocephalosporanic acid (7-ACA).

61-24-5 - Upstream Downstream Industry

Downstream Products7-Aminocephalosporanic acid
Cefotaxime
Cephalothin sodium
Cefazolin
7-Amino-3-[(5-methyl-1,3,4-thiadiazol-2-ylthio)methyl]-3-cephem-4-carboxylic Acid
(6R-trans)-3-(acetoxymethyl)-8-oxo-7-(1H-tetrazol-1-ylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
deacetoxycephalosporin C

61-24-5 - Uses and synthesis methods

properties

Cephalosporin C (CPC) is a β-lactam antibiotic produced by Cephalosporium acropora (Acremoniumchrysogenum). The structure shows that cephalosporin C uses a dihydrothiazine ring to replace the thiazole ring in penicillin and is connected to the β-lactam ring. It is precisely because of this structural difference that cephalosporin C has stronger stability. It is not easy to be destroyed by penicillinase and can kill many penicillin-resistant bacteria.

production method

produced by fermentation.

Last Update:2024-04-09 15:16:16
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Shanghai Macklin Biochemical Co., Ltd
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Product Name: (6R,7R)-3-(Acetoxymethyl)-7-((R)-5-amino-5-carboxypentanamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Visit Supplier Webpage Request for quotation
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View History
61-24-5
2-NONYNOIC ACID ETHYL ESTER
9003-36-5
1172-76-5
SEC-BUTYL
c3172
Pelargonaldehyde
AcetoAcet-P-ChlorolAnilide
ALKANE C34
CH3OCOCOOCH3
Downstream Products for 61-24-5
Cefotaxime
Cephalothin sodium
7-Amino-3-[(5-methyl-1,3,4-thiadiazol-2-ylthio)methyl]-3-cephem-4-carboxylic Acid
(6R-trans)-3-(acetoxymethyl)-8-oxo-7-(1H-tetrazol-1-ylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
deacetoxycephalosporin C
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