74785-89-0

Basic information

• Product Name: Methyl 4-(phenylseleno)butanoate
• Synonyms: Methyl 4-(phenylseleno)butanoate
• CAS NO: 74785-89-0
• Molecular Weight: 257.191
• Mol File: 74785-89-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Methyl 4-(phenylseleno)butanoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 4-(phenylseleno)butanoate(74785-89-0)
• EPA Substance Registry System: Methyl 4-(phenylseleno)butanoate(74785-89-0)

Safety Data

• Hazardous Substances Data: 74785-89-0(Hazardous Substances Data)

Upstream product

• 1666-13-3 diphenyl diselenide 
• 23974-72-3 sodium phenylselenide 
• 23768-06-1 4-(phenylseleno)butanoic acid 
• 67-56-1 methanol 
• 104680-44-6 4-(phenylseleno)butanoyl chloride 
• 2179-79-5 phenyl selenocyanate 
• 4897-84-1 Methyl 4-bromobutyrate 
• 66003-76-7 Diphenyliodonium triflate 

Downstream Products

• 3724-55-8 methyl but-3-enoate 
• 124854-74-6 4-(Phenylseleno)butanal 
• 1447846-70-9 1,1-bis(4-chlorophenyl)-4-(phenylseleno)butan-1-ol 
• 124781-76-6 (5α,8ξ)-5,8-Dihydro-5-methoxy-7-methyl-2-phenyl-8-<3-(phenylseleno)propyl>-s-triazolo<1.2-a>pyridazine-1,3-dione 
• 124781-71-1 Methyl (E)-2-Methyl-6-(phenylseleno)-2-hexenoate 
• 124781-84-6 2-<3-(Phenylseleno)propyl>-2,3-dihydropyran-4-one 
• 124781-70-0 (1Ξ,6E)-1-Methoxy-3-methyl-7-(phenylseleno)hepta-1,3-diene 
• 124781-73-3 (E)-2-Methyl-6-(phenylseleno)-2-hexanal 
• 124781-72-2 (E)-2-Methyl-6-(phenylseleno)-2-hexen-1-ol 

Relevant articles and documents

Metal-free synthesis of unsymmetrical organoselenides and selenoglycosides

A one-pot, metal-free procedure has been developed to synthesize unsymmetrical organoselenides. In the first step of the reaction, arylation of potassium selenocyanate (KSeCN) with an iodonium reagent proceeds in the absence of a metal catalyst to produce

Formal α-Vinylation of Amino Acids. Use of a New Benzeneselenolate Equivalent

A new synthetic approach to the formal α-vinylation of α-amino acids is described, in which the readily available electrophile, ethylene oxide, serves as the vinyl cation equivalent.N-Benzoyl α-amino esters bearing appropriate side-chain protecting groups