97780-98-8

Basic information

• Product Name: 3-(2-Cyanophenyl)-2-methylprop-1-ene
• Synonyms: 2-(2-Methylallyl)benzonitrile;3-(2-Cyanophenyl)-2-methylprop-1-ene
• CAS NO: 97780-98-8
• Molecular Formula: C₁₁H₁₁N
• Molecular Weight: 157.22
• Mol File: 97780-98-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 246.7°C at 760 mmHg
• Flash Point: 103°C
• Appearance: /
• Density: 0.97g/cm³
• Vapor Pressure: 0.0267mmHg at 25°C
• Refractive Index: 1.526
• CAS DataBase Reference: 3-(2-Cyanophenyl)-2-methylprop-1-ene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-Cyanophenyl)-2-methylprop-1-ene(97780-98-8)
• EPA Substance Registry System: 3-(2-Cyanophenyl)-2-methylprop-1-ene(97780-98-8)

Safety Data

• Hazardous Substances Data: 97780-98-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H11N/c1-9(2)7-10-5-3-4-6-11(10)8-12/h3-6H,1,7H2,2H3

Upstream product

• 1458-98-6 2-methyl-3-bromo-1-propene 
• 2042-37-7 o-cyanobromobenzene 
• 18292-38-1 2-methallyltrimethylsilane 
• 91-15-6 phthalonitrile 

Downstream Products

• 10489-28-8 2,2-dimethyl-indan-1-one 
• 1296867-40-7 trans-(P(n)Bu₃)2Ni(C₆H₄-CH₂C(CH₃)=CH₂)(CN*Al(CH₃)2Cl) 
• 1296867-50-9 C₁₉H₂₃NSi 

Relevant articles and documents

Copper-Catalyzed Redox-Triggered Remote C-H Functionalization: Highly Selective Formation of C-CF3 and C-O Bonds

A Cu-catalyzed remote sp3 C-H/unactivated alkenes functionalization reaction for the concomitant construction of C-CF3 and C-O bonds was described. An 1,5-H radical transfer involving an sp3 C-H bond adjacent to a nitrogen atom and an α-CF3-alkyl radical intermediate derived from unactivated alkenes was observed and demonstrated to proceed via the radical process. C-CF3 formation/1,5-H radical shift/remote functionalization of sp3 C-H bond.

Phosphine-catalyzed remote β-C-H functionalization of amines triggered by trifluoromethylation of alkenes: One-pot synthesis of bistrifluoromethylated enamides and oxazoles

An unprecedented phosphine-catalyzed remote β-C-H functionalization of amine derivatives triggered by trifluoromethylation of an alkene with Togni's reagent was disclosed. This reaction proceeded through the highly selective and concomitant activation of

A NOVEL PHOTOSUBSTITUTION OF DICYANOBENZENES BY ALLYLIC AND BENZYLIC SILANES

The photosubstitution of o- and p-dicyanobenzenes by allylic and benzylic silanes in acetonitrile occurred efficiently, giving the corresponding mono-allylated and benzylated cyanobenzenes.