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cefaloram

cefaloram Structure
cefaloram structure
CAS No.
859-07-4
Chemical Name:
cefaloram
Synonyms
cefaloram;Cephalosporin G;(7R)-7-(Phenylacetylamino)-3-(acetoxymethyl)cepham-3-ene-4-carboxylic acid;(7R)-3-(Acetoxymethyl)-7β-[(α-oxophenethyl)amino]cepham-3-ene-4-carboxylic acid;(6R,7R)-3-(Acetoxymethyl)-8-oxo-7-[(phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;(6R,7R)-3-(acetoxymethyl)-8-keto-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;(6R,7R)-3-(acetyloxymethyl)-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;(6R,7R)-3-(acetyloxymethyl)-8-oxo-7-(2-phenylethanoylamino)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[(acetyloxy)methyl]-8-oxo-7-[(2-phenylacetyl)amino]-, (6R,7R)-
CBNumber:
CB0918949
Molecular Formula:
C18H18N2O6S
Molecular Weight:
390.41
MDL Number:
MOL File:
859-07-4.mol
Last updated:2023-05-04 17:34:43
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cefaloram Properties

Melting point 160-162 °C (decomp)
Boiling point 742.8±60.0 °C(Predicted)
Density 1.48±0.1 g/cm3(Predicted)
pka 2.68±0.50(Predicted)
FDA UNII K3086GQJ9Z

cefaloram price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0010951 CEFALORAM 95.00% 859-07-4 5MG $502.9 2021-12-16 Buy
Product number Packaging Price Buy
API0010951 5MG $502.9 Buy

cefaloram Chemical Properties,Uses,Production

Definition

ChEBI: Cefaloram is a cephalosporin derivative with potent antibacterial activity which binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division, inactivation of which interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity, resulting in the weakening of the bacterial cell wall and causing cell lysis. It has a role as an antibacterial drug.

cefaloram synthesis

957-68-6
103-80-0
859-07-4
Synthesis of cefaloram from 7-Aminocephalosporanic acid and Phenylacetyl chloride

cefaloram Preparation Products And Raw materials

Raw materials

Preparation Products

cefaloram Suppliers

Global( 5)Suppliers
Supplier Tel Email Country ProdList Advantage
ShenZhen Trendseen Biological Technology Co.,Ltd. 		13417589054 trendseenbio@gmail.com China 11681 58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 17691182729 18161915376 1046@dideu.com China 10008 58
ShenZhen Trendseen Biological Technology Co.,Ltd. 13417589054 13417589054 trendseenbio@gmail.com China 8941 58
Z-trans Biochemistry Technology (Suzhou) Co.,Ltd 0512-66317708 13372112871 huijuan@zitrans.cn China 1666 58
Supplier Advantage
ShenZhen Trendseen Biological Technology Co.,Ltd. 		58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 58
ShenZhen Trendseen Biological Technology Co.,Ltd. 58
Z-trans Biochemistry Technology (Suzhou) Co.,Ltd 58

859-07-4(cefaloram)Related Search:

cefaloglycin 7-Amino-3-methoxy-3-cephem-4-carboxylic acid 7-Phenyl-acetamido-deacetoxy-cephalosporanic-acid Hydroxymethyl-7-Aminocephalosporanic acid 7-AMCA
7-Aminocephalosporanic acid 3-ACETOXYMETHYL-7-AMINO-8-OXO-5-THIA-1-AZA-BICYCLO[4.2.0]OCT-2-ENE-2-CARBOXYLIC ACID cefaloram

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cefaloram Cephalosporin G (6R,7R)-3-(Acetoxymethyl)-8-oxo-7-[(phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (7R)-3-(Acetoxymethyl)-7β-[(α-oxophenethyl)amino]cepham-3-ene-4-carboxylic acid (7R)-7-(Phenylacetylamino)-3-(acetoxymethyl)cepham-3-ene-4-carboxylic acid (6R,7R)-3-(acetoxymethyl)-8-keto-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (6R,7R)-3-(acetyloxymethyl)-8-oxo-7-(2-phenylethanoylamino)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (6R,7R)-3-(acetyloxymethyl)-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[(acetyloxy)methyl]-8-oxo-7-[(2-phenylacetyl)amino]-, (6R,7R)- 859-07-4