313969-96-9

Basic information

• Product Name: (S)-2-(Allyl-{2-[allyl-((S)-1-methoxycarbonyl-3-methyl-butyl)-carbamoyl]-benzoyl}-amino)-4-methyl-pentanoic acid methyl ester
• Synonyms: (S)-2-(Allyl-{2-[allyl-((S)-1-methoxycarbonyl-3-methyl-butyl)-carbamoyl]-benzoyl}-amino)-4-methyl-pentanoic acid methyl ester
• CAS NO: 313969-96-9
• Molecular Weight: 500.635
• Mol File: 313969-96-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-(Allyl-{2-[allyl-((S)-1-methoxycarbonyl-3-methyl-butyl)-carbamoyl]-benzoyl}-amino)-4-methyl-pentanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(Allyl-{2-[allyl-((S)-1-methoxycarbonyl-3-methyl-butyl)-carbamoyl]-benzoyl}-amino)-4-methyl-pentanoic acid methyl ester(313969-96-9)
• EPA Substance Registry System: (S)-2-(Allyl-{2-[allyl-((S)-1-methoxycarbonyl-3-methyl-butyl)-carbamoyl]-benzoyl}-amino)-4-methyl-pentanoic acid methyl ester(313969-96-9)

Safety Data

• Hazardous Substances Data: 313969-96-9(Hazardous Substances Data)

Upstream product

• 88-95-9 Phthaloyl dichloride 
• 73270-65-2 N-allylated leucine methyl ester 

Relevant articles and documents

The synthesis of sterically demanding amino acid-derived cyclic phosphonamides

The preparation and utilization of C2-symmetric 1,4-diamines in the synthesis of amino acid-derived cyclic phosphonamides 1-3 are described. The 1,4-diamines are synthesized via three methods: (i) amino acid/fumaryl chloride coupling followed by amide reduction, (ii) amino acid/1,4-diamine coupling followed by amide reduction, and (iii) a template-supported ring-closing metathesis/hydrolysis sequence. The pseudo C2-symmetric cyclic phosphonamides 1-3 are prepared by condensation of the C2-symmetric 1,4-diamines to P(III) centers, followed by oxidation.