1235453-06-1

Basic information

• Product Name: tert-butyl (2S,3'S)-1-(3'-benzyloxycarbonylamino-4'-tert-butoxy-4'-oxobutanethioyl)azetidine-2-carboxylate
• Synonyms: tert-butyl (2S,3'S)-1-(3'-benzyloxycarbonylamino-4'-tert-butoxy-4'-oxobutanethioyl)azetidine-2-carboxylate
• CAS NO: 1235453-06-1
• Molecular Weight: 478.61
• Mol File: 1235453-06-1.mol

Chemical Properties

• CAS DataBase Reference: tert-butyl (2S,3'S)-1-(3'-benzyloxycarbonylamino-4'-tert-butoxy-4'-oxobutanethioyl)azetidine-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (2S,3'S)-1-(3'-benzyloxycarbonylamino-4'-tert-butoxy-4'-oxobutanethioyl)azetidine-2-carboxylate(1235453-06-1)
• EPA Substance Registry System: tert-butyl (2S,3'S)-1-(3'-benzyloxycarbonylamino-4'-tert-butoxy-4'-oxobutanethioyl)azetidine-2-carboxylate(1235453-06-1)

Safety Data

• Hazardous Substances Data: 1235453-06-1(Hazardous Substances Data)

Downstream Products

• 1235453-07-2 tert-butyl (2S,3'S)-1-(3'-benzyloxycarbonylamino-4'-tert-butoxy-4'-oxobutyl)azetidine-2-carboxylate 

Relevant articles and documents

Determination of the structure and its absolute configuration of 2″-hydroxynicotianamine, an inhibitor against Angiotensin-I converting enzyme in buckwheat, through the total synthesis

Nicotianamine is known as an inhibitor against Angiotensin-I Converting Enzyme (ACE). We synthesized a new nicotianamine derivative with an additional hydroxy group isolated from buckwheat (Fagopyrum esculentum Moench) powder and determined its regio and stereochemistry unambiguously by the enantioselective synthesis of diastereomers.