cephamycin C

Base Information

Chemical Name:cephamycin C
CAS No.:32178-84-0
Molecular Formula:C₁₆H₂₂N₄O₉S
Molecular Weight:446.438
Hs Code.:

Synonyms:cephamycin C

Suppliers and Price of cephamycin C

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

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Chemical Property of cephamycin C

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:: SDS file from LookChem

Useful:

Technology Process of cephamycin C

There total 1 articles about cephamycin 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:

: 32178-84-0,34279-51-1,38429-35-5,39212-31-2,64162-09-0
(6R)-7t-((R)-5-amino-5-carboxy-pentanoylamino)-3-carbamoyloxymethyl-7c-methoxy-8-oxo-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Guidance literature:: Streptomyces Lactamdurans (MA 2908);

Reference yield:

: 32178-84-0
cephamycin C

: 35607-66-0
cefoxitin

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) N-trichloroethoxycarbonylation, 2.) benzhydryl esterification

2: 1.) Na₂CO₃, 2.) H₂O / 1.) dioxane, 5 deg C, then 20 deg C, 12 h, 2.) 1 h

3: 1.) PhN=C=NPh, 2.) N,N-dimethylaniline / 1.) CH₂Cl₂, 18 h, 0 deg C, 2.) CH₂Cl₂

4: 56 percent / CF₃COOH / various solvent(s) / 1.) -30 deg C, 2.) -20 deg C, 20 min, 3.) -10 deg C, 20 min

With water; sodium carbonate; N,N-dimethyl-aniline; 1,3-Diphenylcarbodiimide; trifluoroacetic acid; In various solvent(s);
DOI:10.1016/0040-4020(80)80149-9

Reference yield:

: 32178-84-0
cephamycin C

: 35607-68-2
diphenylmethyl (6R, 7S)-7-(2'-thienyl)acetamido-7-methoxy-3-carbamoyloxymethyl-3-cephem-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) N-trichloroethoxycarbonylation, 2.) benzhydryl esterification

2: 1.) Na₂CO₃, 2.) H₂O / 1.) dioxane, 5 deg C, then 20 deg C, 12 h, 2.) 1 h

3: 1.) PhN=C=NPh, 2.) N,N-dimethylaniline / 1.) CH₂Cl₂, 18 h, 0 deg C, 2.) CH₂Cl₂

With water; sodium carbonate; N,N-dimethyl-aniline; 1,3-Diphenylcarbodiimide;
DOI:10.1016/0040-4020(80)80149-9