40506-75-0

Basic information

• Product Name: (6R,7R)-3-benzyl-7-(thien-2-ylacetamido)-ceph-3-em-4-carboxylic acid
• Synonyms: (6R,7R)-3-benzyl-7-(thien-2-ylacetamido)-ceph-3-em-4-carboxylic acid
• CAS NO: 40506-75-0
• Molecular Weight: 414.506
• Mol File: 40506-75-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (6R,7R)-3-benzyl-7-(thien-2-ylacetamido)-ceph-3-em-4-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (6R,7R)-3-benzyl-7-(thien-2-ylacetamido)-ceph-3-em-4-carboxylic acid(40506-75-0)
• EPA Substance Registry System: (6R,7R)-3-benzyl-7-(thien-2-ylacetamido)-ceph-3-em-4-carboxylic acid(40506-75-0)

Safety Data

• Hazardous Substances Data: 40506-75-0(Hazardous Substances Data)

Upstream product

• 40506-72-7 (6R)-7t-amino-3-benzyl-8-oxo-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid tert-butyl ester; toluene-4-sulfonate 
• 591-51-5 phenyllithium 
• 39098-97-0 2-thienylacetic acid chloride 
• 53674-03-6 2,2,2-trichloroethyl(6R,7R)-3-benzyl-7-(thien-2-ylacetamido)-ceph-3-em-4-carboxylate 
• 33465-56-4 2,2,2-trichloroethyl (1S,6R,7R)-3-bromomethyl-7-formamidoceph-3-em-4-carboxylate 1-oxide 
• 53673-98-6 2,2,2-trichloroethyl(1S,6R,7R)-7-amino-3-benzylceph-3-em-4-carboxylate 1-oxide hydrochloride 
• 53683-56-0 2,2,2-trichloroethyl(1S,6R,7R)-3-benzyl-7-(thien-2-ylacetamido)ceph-3-em-4-carboxylate 1-oxide 
• 53673-97-5 2,2,2-trichloroethyl(1S,6R,7R)-3-benzyl-7-formamidoceph-3-em-4-carboxylate 1-oxide 
• 40506-74-9 (6R)-3-benzyl-8-oxo-7t-(2-thiophen-2-yl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid tert-butyl ester 

Relevant articles and documents

Synthesis of 3-functionalised cephalosporins by photoinitiated bromination. Transformations of 2,2,2-trichloroethyl 1S, 6R, 7R)-3-bromomethyl-7-formamidoceph-3-EM-4-carboxylate, 1-oxide

The 3-bromomethyl derivative 2c, obtained by photoinitiated bromination of the corresponding 3-Me compound 1c, has been converted into the antibiotics cephalothin 18 and cephaloridine 20. Reaction of 2c with lithium dimethyl- and diphenyl-cuprate led to the intermediates 22 and 24 respectively. Further transformation of 24 provided the 3-benzyl derivative 27, an isostere of cephaloridine.