90173-08-3

Basic information

• Product Name: (Z)-4-Phenyl-hex-4-enoic acid methyl ester
• Synonyms: (Z)-4-Phenyl-hex-4-enoic acid methyl ester
• CAS NO: 90173-08-3
• Molecular Weight: 204.269
• Mol File: 90173-08-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (Z)-4-Phenyl-hex-4-enoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-4-Phenyl-hex-4-enoic acid methyl ester(90173-08-3)
• EPA Substance Registry System: (Z)-4-Phenyl-hex-4-enoic acid methyl ester(90173-08-3)

Safety Data

• Hazardous Substances Data: 90173-08-3(Hazardous Substances Data)

Upstream product

• 1445-45-0 Trimethyl orthoacetate 
• 6249-81-6 3-phenyl-but-3-en-2-ol 
• 1035799-84-8 2-Methyl-3-phenyl-but-3-enoyl chloride 
• 67-56-1 methanol 
• 90172-83-1 1-Diazo-3-methyl-4-phenyl-pent-4-en-2-one 
• 90173-14-1 2-methyl-3-phenylbut-3-enoic acid 

Downstream Products

• 1420480-10-9 (Z)-4-phenylhex-4-en-1-ol 
• 1420480-27-8 C₁₃H₁₈O₃S 
• 1420480-45-0 (E)-3-nitro-N-(4-phenylhex-4-en-1-yl)benzenesulfonamide 
• 1420479-57-7 (S)-2-((S)-1-bromoethyl)-1-((3-nitrophenyl)sulfonyl)-2-phenylpyrrolidine 
• 1420479-75-9 (2R,3R)-2-methyl-1-((3-nitrophenyl)sulfonyl)-3-phenylpiperidin-3-ol 
• 1420479-76-0 (R)-6-methyl-1-((3-nitrophenyl)sulfonyl)-5-phenyl-1,2,3,6-tetrahydropyridine 
• 1420479-36-2 (Z)-3-nitro-N-(4-phenylhex-4-en-1-yl)benzenesulfonamide 

Relevant articles and documents

C2-symmetric cyclic selenium-catalyzed enantioselective bromoaminocyclization

A catalytic asymmetric bromocyclization of trisubstituted olefinic amides that uses a C2-symmetric mannitol-derived cyclic selenium catalyst and a stoichiometric amount of N-bromophthalimide is reported. The resulting enantioenriched pyrrolidine products, which contain two stereogenic centers, can undergo rearrangement to yield 2,3-disubstituted piperidines with excellent diastereoselectivity and enantiospecificity.