55283-02-8

Basic information

• Product Name: (E)-6-Phenyl-2-hexenoic acid methyl ester
• Synonyms: (E)-6-Phenyl-2-hexenoic acid methyl ester
• CAS NO: 55283-02-8
• Molecular Formula: C₁₃H₁₆O₂
• Molecular Weight: 204.26
• Mol File: 55283-02-8.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (E)-6-Phenyl-2-hexenoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-6-Phenyl-2-hexenoic acid methyl ester(55283-02-8)
• EPA Substance Registry System: (E)-6-Phenyl-2-hexenoic acid methyl ester(55283-02-8)

Safety Data

• Hazardous Substances Data: 55283-02-8(Hazardous Substances Data)

Upstream product

• 18328-11-5 3-benzyl propionaldehyde 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 
• 1067-74-9 Methyl diethylphosphonoacetate 
• 64283-87-0 4-phenyl-1-iodobutane 
• 888407-59-8 methyl 2-diazo-6-phenylhexanoate 
• 3360-41-6 4-phenyl-butan-1-ol 

Downstream Products

• 5581-76-0 6-phenyl-hexanoic acid methyl ester 
• 117213-97-5 3-(3-Phenyl-propyl)-pentanedioic acid dimethyl ester 
• 16387-61-4 6-phenylhexanal 
• 137650-08-9 α(R)-methylbenzenehexanamine 
• 137650-07-8 2-(methoxymethyl)-N-<1(R)-methyl-6-phenylhexyl>-1-pyrrolidinamine 
• 137650-06-7 2-(methoxymethyl)-N-(6-phenylhexylidene)-1-pyrrolidinamine 
• 137650-44-3 α(S)-amino-4-hydroxy-2,6-dimethyl-N-<1(R)-methyl-6-phenylhexyl>benzenepropanamide 
• 1266551-62-5 (E)-triisopropyl((6-phenylhex-2-en-1-yl)oxy)silane 
• 130127-81-0 (E)-6-phenylhex-2-en-1-ol 

Relevant articles and documents

Ligand-controlled cobalt-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes

The Co-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes were realized by a ligand-controlled strategy. The remote hydroboration with dcype provided borylethers, while xantphos favored the formation of silyl enol ethers.

Tetrahydronaphthalene derivatives by amberlyst 15-promoted friedel-crafts cyclizations

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Enantioselective Hydrolysis of Dialkyl 3-Monosubstituted Glutarates with Pig Liver Esterase: Structure-Optical Purity Relationships

Dialkyl 3-monosubstituted glutarates are subjected to hydrolysis with pig liver esterase to afford the corresponding chiral half-esters.Synnthetically useful half-esters of higher optical purity are obtained from the prochiral substrates of more hydrophob