Cefazolin IMpurity C

Base Information

Chemical Name:Cefazolin IMpurity C
CAS No.:56842-77-4
Molecular Formula:C11H12N6O4S
Molecular Weight:324.32
Hs Code.:

Synonyms:Cefazolin IMpurity C;(6R,7R)-3-methyl-8-oxo-7-[(1H-tetrazol-1-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;Cefazolin EP Impurity C;(6R,7R)-7-(2-(1H-tetrazol-1-yl)acetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Suppliers and Price of Cefazolin IMpurity C

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
7-[1-(1H)-Tetrazolylacetamido]desacetoxycephalosporanicAcid
10mg
$ 1320.00

TRC
7-[1-(1H)-Tetrazolylacetamido]desacetoxycephalosporanicAcid
5mg
$ 775.00

Total 15 raw suppliers

Chemical Property of Cefazolin IMpurity C

Chemical Property:

PSA：155.61000
LogP:-1.23960
Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere
Solubility.:DMSO (Slightly, Sonicated), TFA (Slightly)

Purity/Quality:

97% ^*data from raw suppliers

7-[1-(1H)-Tetrazolylacetamido]desacetoxycephalosporanicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 7-[1-(1H)-Tetrazolylacetamido]desacetoxycephalosporanic Acid, is an impurity of Cefazolin (C242500), a semi-synthetic antibiotic derived from 7-amino-cephalosporanic acid. An antibacterial.

Technology Process of Cefazolin IMpurity C

There total 1 articles about Cefazolin IMpurity C which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 22252-43-3,26395-99-3,70287-30-8,72059-35-9
3-deacetyloxy-7-aminocephalosporanic acid

: 55633-19-7
(1H-tetrazol-1-yl)-2-acetic acid methyl ester

: 21732-17-2
1H-tetrazol-1-ylacetic acid

: 56842-77-4
7-<1-(1H)-tetrazolylacetamido>-3-methyl-Δ³-cephem-4-carboxylic acid

Guidance literature:: With immobilized penicillin G acylase from Escherichia coli; In phosphate buffer; at 4 ℃; pH=6.5; Kinetics;
DOI:10.1002/adsc.200404136