489432-91-9

Basic information

• Product Name: (S)-2-[((E)-But-2-enoyl)-(4-methoxy-benzyl)-amino]-5-hydroxy-pentanoic acid methyl ester
• CAS NO: 489432-91-9
• Molecular Weight: 335.4
• Mol File: 489432-91-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-[((E)-But-2-enoyl)-(4-methoxy-benzyl)-amino]-5-hydroxy-pentanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-[((E)-But-2-enoyl)-(4-methoxy-benzyl)-amino]-5-hydroxy-pentanoic acid methyl ester(489432-91-9)
• EPA Substance Registry System: (S)-2-[((E)-But-2-enoyl)-(4-methoxy-benzyl)-amino]-5-hydroxy-pentanoic acid methyl ester(489432-91-9)

Safety Data

• Hazardous Substances Data: 489432-91-9(Hazardous Substances Data)

Upstream product

• 489432-90-8 (S)-2-[((E)-But-2-enoyl)-(4-methoxy-benzyl)-amino]-pentanedioic acid 5-tert-butyl ester 1-methyl ester 
• 344765-07-7 2-(4-methoxy-benzylamino)-pentanedioic acid 5-tert-butyl ester 1-methyl ester 
• 56877-41-9 methyl 2(S)-2-benzyloxycarbonylamino-4-tert-butoxycarbonylbutanoate 
• 53838-27-0 H-Glu(tBu)-OMe 

Downstream Products

• 489432-92-0 (E)-But-2-enoic acid ((S)-2-hydroxy-tetrahydro-pyran-3-yl)-(4-methoxy-benzyl)-amide 

Relevant articles and documents

TBAT-mediated nitrone formation of ω-mesyloxy-O-tert-butyldiphenylsilyloximes: Facile synthesis of cyclic nitrones from hemiacetals

Chiral and cyclic nitrones were synthesized by TBAT-mediated desilylative cyclization of ω-mesyloxy-O-tert-butyl-diphenylsilyloximes, readily prepared from sugar derivatives by a consecutive treatment with O-tert-butyldiphenylsilylhydroxylamine and with m