61463-62-5

Basic information

• Product Name: 3-(3-CYANOPHENYL)-1-PROPENE
• Synonyms: 3-(3-CYANOPHENYL)-1-PROPENE;3-allylbenzonitrile
• CAS NO: 61463-62-5
• Molecular Formula: C₁₀H₉N
• Molecular Weight: 143.19
• Mol File: 61463-62-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 234.7°C at 760 mmHg
• Flash Point: 95.6°C
• Appearance: /
• Density: 0.99g/cm³
• Vapor Pressure: 0.0522mmHg at 25°C
• Refractive Index: 1.534
• CAS DataBase Reference: 3-(3-CYANOPHENYL)-1-PROPENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-CYANOPHENYL)-1-PROPENE(61463-62-5)
• EPA Substance Registry System: 3-(3-CYANOPHENYL)-1-PROPENE(61463-62-5)

Safety Data

• Hazardous Substances Data: 61463-62-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H9N/c1-2-4-9-5-3-6-10(7-9)8-11/h2-3,5-7H,1,4H2

Upstream product

• 18257-89-1 1-allyl-3-bromo-benzene 
• 544-92-3 copper(I) cyanide 
• 6952-59-6 3-cyanobromobenzene 
• 24850-33-7 allyltributylstanane 
• 106-95-6 allyl bromide 
• 626-17-5 benzene-1,3-dicarbonitrile 
• 2237-30-1 m-cyanoaniline 
• 762-72-1 allyl-trimethyl-silane 

Downstream Products

• 83101-13-7 3-(3-cyanophenyl)-1-propanol 
• 655251-03-9 C₂₁H₃₃N₃O₅ 
• 655251-06-2 C₂₂H₃₅N₃O₇S 
• 74254-14-1 trans-1-(3-cyanophenyl)prop-1-ene 

Relevant articles and documents

Photo-Ni-Dual-Catalytic C(sp2)-C(sp3) Cross-Coupling Reactions with Mesoporous Graphitic Carbon Nitride as a Heterogeneous Organic Semiconductor Photocatalyst

The synergistic combination of a heterogeneous organic semiconductor mesoporous graphitic carbon nitride (mpg-CN) and a homogeneous nickel catalyst with visible-light irradiation at room temperature affords the C(sp2)-C(sp3) cross-co

Chemo- and regioselective reductive transposition of allylic alcohol derivatives via iridium or rhodium catalysis

We report highly chemo- and regioselective reductive transpositions of methyl carbonates to furnish olefin products with complementary regioselectivity to that of established Pd-catalysis. These Rh- and Ir-catalysed transformations proceed under mild conditions and enable selective deoxygenation in the presence of functional groups that are susceptible to reduction by metal hydrides.

Method of preparing organomagnesium compounds

The present invention is directed to a reagent for use in the preparation of organomagnesium compounds as well as to a method of preparing such organomagnesium compounds. The present invention furthermore provides a method of preparing functionalized or unfunctionalized organic compounds as well as the use of the reagents of the present invention in the preparation of organometallic compounds and their reaction with electrophiles. Finally, the present invention is directed to the use of lithium salts - LiY in the preparation of organometallic compounds and their reactions with electrophiles and to an organometallic compound which is obtainable by the disclosed method.