182007-73-4

Basic information

• Product Name: (S)-3-((2E,4E)-Hexa-2,4-dienoylamino)-3-phenyl-propionic acid tert-butyl ester
• Synonyms: (S)-3-((2E,4E)-Hexa-2,4-dienoylamino)-3-phenyl-propionic acid tert-butyl ester
• CAS NO: 182007-73-4
• Molecular Weight: 315.412
• Mol File: 182007-73-4.mol

Chemical Properties

• CAS DataBase Reference: (S)-3-((2E,4E)-Hexa-2,4-dienoylamino)-3-phenyl-propionic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-((2E,4E)-Hexa-2,4-dienoylamino)-3-phenyl-propionic acid tert-butyl ester(182007-73-4)
• EPA Substance Registry System: (S)-3-((2E,4E)-Hexa-2,4-dienoylamino)-3-phenyl-propionic acid tert-butyl ester(182007-73-4)

Safety Data

• Hazardous Substances Data: 182007-73-4(Hazardous Substances Data)

Upstream product

• 110-44-1 sorbic Acid 
• 120686-18-2 (S)-3-amino-3-phenylpropionic acid tert-butyl ester 
• 151133-00-5 tert-butyl (3S,αR)-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-phenylpropanoate 
• 14990-09-1 tert-butyl cinnamate 
• 110-44-1 hexa-2,4-dienoic acid 

Downstream Products

• 182007-72-3 (S)-3-((2E,4E)-Hexa-2,4-dienoylamino)-3-phenyl-propionic acid 

Relevant articles and documents

Asymmetric syntheses of moiramide B and andrimid

The first highly diastereoselective asymmetric syntheses of moiramide B 2 and andrimid 3 have been achieved using lithium amide (R)-6 and pyrrolidinone auxiliary (R)-9. Pyrrolidinone auxiliary (R)-9 was used to create the novel (S)-3-methyl-N-benzyloxysuc

Asymmetric synthesis of moiramide B

The first asymmetric synthesis of Moiramide B 1 is achieved using lithium amide 4 and pyrrolidinone auxiliary 5; pyrrolidinone auxiliary 5 is used to create the novel (S)-2-methyl-N-benzyloxysuccinimide 15 which is subsequently acylated with the highly re