130517-98-5

Basic information

• Product Name: methyl N-[(4S)-4-phenylbut-1-en-4-yl]-(S)-valinate
• Synonyms: methyl N-[(4S)-4-phenylbut-1-en-4-yl]-(S)-valinate
• CAS NO: 130517-98-5
• Molecular Weight: 261.364
• Mol File: 130517-98-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: methyl N-[(4S)-4-phenylbut-1-en-4-yl]-(S)-valinate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl N-[(4S)-4-phenylbut-1-en-4-yl]-(S)-valinate(130517-98-5)
• EPA Substance Registry System: methyl N-[(4S)-4-phenylbut-1-en-4-yl]-(S)-valinate(130517-98-5)

Safety Data

• Hazardous Substances Data: 130517-98-5(Hazardous Substances Data)

Upstream product

• 18925-10-5 allylzinc bromide 
• 130608-02-5 methyl N-benzylidene-L-valinate 
• 688-61-9 Triallylborane 
• 4070-48-8 L-Valine methyl ester 
• 13803-83-3 methyl (S)-2-(benzylideneamino)-3-methylbutanoate 
• 106-95-6 allyl bromide 
• 100-52-7 benzaldehyde 
• 6306-52-1 L-valine methylester hydrochloride 
• 133834-87-4 3-bromo-1-iodo-(E)-1-propene 
• 2622-05-1 allylmagnesium bromide 

Downstream Products

• 4383-23-7 (S)-1-phenylbut-3-en-1-amine 
• 154228-41-8 (2S)-3-methyl-2-((1S)-1-phenylbut-3-enylamino)butan-1-ol 
• 949021-19-6 (S)-N-(1-phenyl-3-buten-1-yl)propenamide 

Relevant articles and documents

A Modification of the Hiyama Reaction. Synthesis of Homo Allylic Amines from Imines and Allylic Bromides in the Presence of CrCl2

Arylic and alkylic imines, activated with BF3*OEt2 react with different allylic bromides in the presence of CrCl2 to give the corresponding homo allylic amines.The reaction can be performed in a single step starting from the aldehyde and the amine, in the

Electrochemical allylation reactions of simple imines in aqueous solution mediated by nanoscale zinc architectures

I zinc we're alone now: The title reactions were achieved in an undivided cell fitted with a pair of zinc electrodes in aqueous solution. A preliminary study on the relationship of reaction activity and surface morphology showed that the deposited zinc powders with nanoscale architectures had very high activity.

Reaction of allylic-type diindium compounds with electrophiles

Allylic-type diindium reagents were prepared from 3-bromo-1-iodopropene (1a), 3-bromo-1-iodo-1-phenylpropene (1b), or 2,4-diiodobut-2-en-1-ol (1c) with metallic indium, and their successive coupling with electrophiles was examined. The coupling behavior o