872513-93-4

Basic information

• Product Name: (2S)-methyl 2-N-benzoylamino-5-methylhex-4-enoate
• Synonyms: (2S)-methyl 2-N-benzoylamino-5-methylhex-4-enoate
• CAS NO: 872513-93-4
• Molecular Weight: 261.321
• Mol File: 872513-93-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2S)-methyl 2-N-benzoylamino-5-methylhex-4-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-methyl 2-N-benzoylamino-5-methylhex-4-enoate(872513-93-4)
• EPA Substance Registry System: (2S)-methyl 2-N-benzoylamino-5-methylhex-4-enoate(872513-93-4)

Safety Data

• Hazardous Substances Data: 872513-93-4(Hazardous Substances Data)

Upstream product

• 120341-28-8 Methyl 2-(N-Benzoylamino)-2-(dimethoxyphosphinyl)ethanoate 
• 21286-78-2 methyl N-benzoyl-2-methoxyglycinate 
• 19791-95-8 α-hydroxyhippuric acid 
• 55-21-0 benzamide 
• 947154-56-5 (2Z)-methyl 2-N-benzoylamino-5-methylhexa-2,4-dienoate 
• 180470-61-5 (2S)-methyl 2-N-benzoylaminopent-4-enoate 
• 115-11-7 isobutene 

Downstream Products

• 947154-84-9 (2S)-6-acetoxy-2-benzoylamino-4-hexenoic acid methyl ester 
• 1440507-70-9 (S,E)-methyl 2-benzamido-5,6-dimethylhept-4-enoate 
• 872513-99-0 (2S,7S)-dimethyl 2,7-N,N-dibenzoylaminooct-4-enedioate 
• 872513-95-6 (2S)-methyl 2-N-benzoylaminohex-4-enoate 

Relevant articles and documents

A one pot, metathesis-hydrogenation sequence for the selective formation of carbon-carbon bonds

A combination of homogeneous hydrogenation and metathesis reactions allows highly efficient, stepwise chemo- and stereo-selective formation of three separate 2,7-diaminosuberic acid derivatives in a single pot without isolation of intermediates. The Royal

An efficient protocol for the cross-metathesis of sterically demanding olefins

Cross-metathesis of a wide range of previously unreactive, sterically demanding alkenes can be achieved in fair to excellent yield using a commercially available catalyst by a facile strategy involving reversal of steric preference.