3360-53-0

Basic information

• Product Name: 1-BROMO-2-PHENYL-PROPENE
• Synonyms: 1-BROMO-2-PHENYL-PROPENE
• CAS NO: 3360-53-0
• Molecular Formula: C₉H₉Br
• Molecular Weight: 197.07
• Mol File: 3360-53-0.mol
• Article Data: 18

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-BROMO-2-PHENYL-PROPENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMO-2-PHENYL-PROPENE(3360-53-0)
• EPA Substance Registry System: 1-BROMO-2-PHENYL-PROPENE(3360-53-0)

Safety Data

• Hazardous Substances Data: 3360-53-0(Hazardous Substances Data)

Usage

Appearance

Colorless to yellow liquid The compound's appearance ranges from colorless to yellow in its liquid state.

Strong, pungent odor

1-Bromo-2-phenylpropene has a noticeable and pungent smell.

Primary use

Intermediate in synthesis The compound is mainly used as an intermediate in the production of pharmaceuticals and agrochemicals.

Additional uses

Reagent in organic synthesis, building block in specialty chemicals It also serves as a reagent in organic synthesis and as a building block for creating specialty chemicals.

Flammability

Flammable 1-Bromo-2-phenylpropene is considered to be flammable, which requires caution during handling and storage.

Upstream product

• 60014-86-0 (2,2-dibromo 1-methylethenyl)benzene 
• 98-86-2 acetophenone 
• 100-52-7 benzaldehyde 
• 98-83-9 isopropenylbenzene 
• 704-79-0 3-phenylbut-2-enoic acid 
• 1034-49-7 (bromomethyl)triphenyl phosphonium bromide 
• 31778-29-7 1-bromo-2-phenylpropan-2-ol 
• 704-80-3 (E)-3-phenyl-2-butenoic acid 
• 60014-81-5 1,2-dibromo-2-trimethylsilyloxy-prop-2-yl-benzene 

Downstream Products

• 98-86-2 acetophenone 
• 16917-35-4 (E)-(1-bromoprop-1-en-2-yl)benzene 
• 19647-26-8 (Z)-β-bromo-α-methylstyrene 
• 1446421-64-2 methyl 3-(2-phenylallyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5-carboxylate 
• 1429762-91-3 C₂₁H₁₉OP 
• 1356829-59-8 3-(4-chlorophenyl)-5-methyl-5-phenyl-2-cyclopentenone 
• 1356829-69-0 3-cyclopropyl-5-methyl-5-phenyl-2-cyclopentenone 
• 1356829-80-5 (5S)-3-(4-chlorophenyl)-5-methyl-5-phenyl-2-cyclopentenone 
• 1356829-58-7 5-methyl-3,5-diphenyl-2-cyclopentenone 
• 4469-66-3 4-Phenyl-2-methoxycarbonyl-4-enoic acid methyl ester 
• 112635-55-9 4-((E)-3-Bromo-2-phenyl-allyloxy)-biphenyl 
• 112635-51-5 1-((E)-3-Bromo-2-phenyl-allyloxy)-2,4-dichloro-benzene 
• 112635-53-7 1-((E)-3-Bromo-2-phenyl-allyloxy)-4-methoxy-benzene 
• 112635-59-3 3,6-Diphenyl-2H-chromene 

Relevant articles and documents

Highly selective hydrosilylation of equilibrating allylic azides

The Pt-catalyzed hydrosilylation of equilibrating allylic azides is reported. The reaction provides only one out of four possible hydrosilylation products in good yields and with very high chemoselectivity (alk-1-enevs.alk-2-ene), regioselectivity (linearvs.branched), and excellent functional group tolerance.

Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

Intramolecular [2+2] photocycloaddition reactions of diversely substituted N-Boc protected 4-(allylaminomethyl)-2(5H)-furanones resulted in rigid products (53-75%) with three spatially defined positions for further functionalisation. The Royal Society of Chemistry.

NOVEL PHOTOINITIATORS AND THEIR APPLICATIONS

Photoinitiators of formula (Ia) or (Ib) having chain transfer groups, wherein n is 1 or 2; PI is for example a group of formula (IIa); PI' inter alia is a group of formula (IIIa); Ar is for example phenyl; Ar2 is inter alia phenylene; R1 and R2 are for ex