77597-25-2

Basic information

• Product Name: p-nitrobenzyl 3-<(3-hydroxypropyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate
• Synonyms: p-nitrobenzyl 3-<(3-hydroxypropyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate
• CAS NO: 77597-25-2
• Molecular Weight: 396.445
• Mol File: 77597-25-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: p-nitrobenzyl 3-<(3-hydroxypropyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: p-nitrobenzyl 3-<(3-hydroxypropyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate(77597-25-2)
• EPA Substance Registry System: p-nitrobenzyl 3-<(3-hydroxypropyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate(77597-25-2)

Safety Data

• Hazardous Substances Data: 77597-25-2(Hazardous Substances Data)

Upstream product

• 77597-23-0 p-nitrobenzyl 3-<<3-(tert-butyldimethylsilyloxy)propyl>thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate 

Downstream Products

• 75527-03-6 p-nitrobenzyl 3-<(3-azidopropyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate 
• 77597-31-0 p-nitrobenzyl 3-<<3-<(1-pyrrolidinylcarbothioyl)thio>propyl>thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate 
• 77597-30-9 p-nitrobenzyl 3-<<3-<(thiocarbamoyl)thio>propyl>thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate 
• 77597-29-6 p-nitrobenzyl 3-<(3-mesyloxypropyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate 
• 77597-26-3 p-nitrobenzyl 3-<(3-acetoxypropyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate 
• 77597-27-4 p-nitrobenzyl 3-<(3-methoxalyloxypropyl)thio>-7-oxo-4-thia-1-azabicyclo<3.2.0>hept-2-ene-2-carboxylate 

Relevant articles and documents

2-(ALKYLTHIO)PENEM-3-CARBOXYLIC ACIDS. II. CHEMICAL MANIPULATION OF PENEM SIDE CHAINS

The tert-butyldimethylsilyl group was found to be effective for protection of the hydroxyl group in penem synthesis.Manipulation of the side-chain hydroxyl group of base-sensitive penem-3-carboxylates was successfully conducted by means of a displacement