24892-82-8

Basic information

• Product Name: 1-bromo-2-(1-phenylpropen-1-yl)benzene
• Synonyms: 1-bromo-2-(1-phenylpropen-1-yl)benzene
• CAS NO: 24892-82-8
• Molecular Weight: 259.145
• Mol File: 24892-82-8.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: 1-bromo-2-(1-phenylpropen-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-2-(1-phenylpropen-1-yl)benzene(24892-82-8)
• EPA Substance Registry System: 1-bromo-2-(1-phenylpropen-1-yl)benzene(24892-82-8)

Safety Data

• Hazardous Substances Data: 24892-82-8(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 583-55-1 1-Bromo-2-iodobenzene 
• 4545-21-5 acetophenone p-toluenesulfonylhydrazone 
• 88-65-3 2-bromobenzoic-acid 
• 899425-05-9 2-bromo-N-methoxy-N-methylbenzamide 
• 2142-69-0 2-bromophenyl methyl ketone 
• 591-17-3 meta-bromotoluene 
• 100-58-3 phenylmagnesium bromide 
• 6630-33-7 ortho-bromobenzaldehyde 
• 13047-06-8 o-bromobenzophenone 
• 20667-19-0 methyltriphenylphosphonium iodide 
• 2065-66-9 methyl-triphenylphosphonium iodide 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 2042-37-7 o-cyanobromobenzene 

Downstream Products

• 906091-57-4 3-phenyl-3-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclobutanone 
• 1335243-44-1 (R)-1-(tert-butylsulfinyl)-2-(1-phenylvinyl)benzene 
• 1379534-67-4 C₂₁H₂₈OSi₂ 
• 1379534-77-6 C₂₁H₂₈OSi₂ 
• 1596361-49-7 C₂₀H₂₂OSi 
• 83947-50-6 2-(2,2-diphenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Relevant articles and documents

Stereocontrolled synthesis of carbon-carbon double bond locked analogues of strobilurins which are characterized by a trans-1,2-disubstituted cyclopropane ring

The racemic forms of four new carbon-carbon double bond locked analogues of strobilurins, which are characterized by a trans-1,2-disubstituted cyclopropane ring, have been synthesized according to a strategy which involves palladium-catalyzed cross-coupli

Enantioselective synthesis of 1-aminoindene derivativesviaasymmetric Br?nsted acid catalysis

We describe a catalytic asymmetric iminium ion cyclization reaction of simple 2-alkenylbenzaldimines using a BINOL-derived chiralN-triflyl phosphoramide. The corresponding 1-aminoindenes and tetracyclic 1-aminoindanes are formed in good yields and high enantioselectivities. Further, the chemical utility of the obtained enantiopure 1-aminoindene is demonstrated for the asymmetric synthesis of (S)-rasagiline.

Preparation method of silicon spiro compound (by machine translation)

The invention discloses a preparation method of a silicon spiro compound. The invention provides a preparation method of a silicon spiro compound as shown in a formula II, which comprises the following steps: in a solvent, a compound represented by the formula III is subjected to cyclization reaction under the presence of a monovalent rhodium catalyst and a phosphine ligand to obtain the silicon spiro compound as shown in the formula II. The preparation method of the silicon spiro compound can be simple. , The establishment of the silicon spiro compound is realized conveniently and efficiently. (by machine translation)