19870-47-4

Basic information

• Product Name: benzylpenicillin-(carbonic acid ethyl ester)-anhydride
• Synonyms: benzylpenicillin-(carbonic acid ethyl ester)-anhydride
• CAS NO: 19870-47-4
• Molecular Weight: 406.459
• Mol File: 19870-47-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: benzylpenicillin-(carbonic acid ethyl ester)-anhydride(CAS DataBase Reference)
• NIST Chemistry Reference: benzylpenicillin-(carbonic acid ethyl ester)-anhydride(19870-47-4)
• EPA Substance Registry System: benzylpenicillin-(carbonic acid ethyl ester)-anhydride(19870-47-4)

Safety Data

• Hazardous Substances Data: 19870-47-4(Hazardous Substances Data)

Upstream product

• 39879-63-5 penicillin-G N-ethylpiperidine salt 
• 541-41-3 chloroformic acid ethyl ester 
• 113-98-4 Penicillin G potassium 

Downstream Products

• 62984-93-4 4-[6β-(2-phenyl-acetylamino)-penicillanoyl]-morpholine 
• 122214-49-7 6β-(2-phenyl-acetylamino)-penicillanic acid-(2-morpholino-ethyl ester) 
• 119621-35-1 6β-(2-phenyl-acetylamino)-penicillanic acid-(3-diethylamino-propyl ester) 
• 122218-31-9 ethyl-bis-{2-[6β-(2-phenyl-acetylamino)-penicillanoyloxy]-ethyl}-amine 
• 809-71-2 6β-(2-phenyl-acetylamino)-penicillanic acid 4-dimethylamino-phenyl ester 
• 69578-02-5 S-phenyl benzylpenicillinthiocarboxylate 
• 80127-23-7 allyl (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 
• 23536-57-4 N-[6β-(2-phenyl-acetylamino)-penicillanoyl]-glycine 
• 3689-73-4 penethacillin 
• 101634-63-3 benzylpenicillin-phenyl ester 
• 1947-61-1 <2S-<2α,5α,6β>>-7-oxo-6-<(phenylacetyl)amino>-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxamide 
• 76055-86-2 <2H3>methyl (3R,4R,7S,12S)-7-methoxycarbonyl-2-oxo-3-phenylacetamido-6,6,11,11-tetramethyl-5,10-dithia-1,8-diazatricyclo<7.3.0^4,8>dodecane-12-carboxylate 
• 76055-85-1 <2H3>methyl (3R,4R,7S,12S)-12-methoxycarbonyl-2-oxo-3-phenylacetamido-6,6,11,11-tetramethyl-5,10-dithia-1,8-diazatricyclo<7.3.0^4,8>dodecane-7-carboxylate 
• 142762-74-1 C₄₈H₅₈N₈O₆S₂ 

Relevant articles and documents

A series of penicillin derived C2-symmetric inhibitors of HIV-1 proteinase: synthesis, mode of interaction, and structure-activity relationships.

The C2-symmetric diester 1 was identified by random screening as a novel inhibitor of HIV-1 proteinase. This led to the preparation of a series of related more potent amides from readily accessible penicillins. Many of the compounds showed potent antivira

Studies related to Penicillins. Part 20. The Mechanism of the Rearangement of Methyl Benzylpenicillinate to Methyl Benzylpenillonate

In boiling benzene containing a trace of iodine, methyl benzylpenicillinate (1) isomerises to methyl benzylpenillonate (10a).The rearrangement is triggered by a 4,7-bond cleavage of the penicillinate (1a) and probably involves the formation of methyl (4S)