1041307-58-7

Basic information

• Product Name: 4-bromo-1-phenylpent-4-en-2-ol
• Synonyms: 4-bromo-1-phenylpent-4-en-2-ol
• CAS NO: 1041307-58-7
• Molecular Weight: 241.128
• Mol File: 1041307-58-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-bromo-1-phenylpent-4-en-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-bromo-1-phenylpent-4-en-2-ol(1041307-58-7)
• EPA Substance Registry System: 4-bromo-1-phenylpent-4-en-2-ol(1041307-58-7)

Safety Data

• Hazardous Substances Data: 1041307-58-7(Hazardous Substances Data)

Upstream product

• 122-78-1 phenylacetaldehyde 
• 513-31-5 2-bromoallyl bromide 
• 7440-66-6 zinc 
• 28557-00-8 phenylzinc chloride 
• 591-51-5 phenyllithium 
• 4747-15-3 1-(2-methoxyvinyl)benzene 

Relevant articles and documents

Enantiomerically Enriched α-Borylzinc Reagents by Nickel-Catalyzed Carbozincation of Vinylboronic Esters

In this paper is described a synthesis of enantiomerically enriched, configurationally stable organozinc reagents by catalytic enantioselective carbozincation of a vinylboronic ester. This process furnishes enantiomerically enriched α-borylzinc intermediates that are shown to undergo stereospecific reactions, producing enantioenriched secondary boronic ester products. The properties of the intermediate α-borylzinc reagent are probed and the synthetic utility of the products is demonstrated by application to the synthesis of (-)-aphanorphine and (-)-enterolactone.

Nucleophilic substitution reaction at an sp2 carbon of vinyl halides with an intramolecular thiol moiety: synthesis of thio-heterocycles

This article presents a full account of intramolecular vinylic substitution reactions of bromoalkenes having an acetylthio moiety, which give sulfur-containing heterocycles such as dihydrothiophene, tetrahydrothiopyran, and 2-alkylidenethietane derivative

Process for producing propargylcarbinol compounds

The present invention provides a process for producing a propargylcarbinol compound of formula (I): STR1 where R1 and R2 are as defined herein. The process comprises reacting a haloallycarbinol compound of formula (II) with a base. The present invention also relates to a process for producing the haloallylcarbinol compound. The above propargylcarbinol compound is useful as an intermediate for agrochemicals, pharmaceuticals, perfumes, resin monomers, and the like.