Chemical Reagents

22364-68-7

  • Product Name:2-Methylbenzyl cyanide
  • Molecular Formula:C9H9N
  • Specifications:99%
  • Molecular Weight:131.177
Inquiry

Product Details;

CasNo: 22364-68-7

Molecular Formula: C9H9N

Appearance: clear colorless to orange-reddish liquid

Top Purity 2-Methylbenzyl cyanide 22364-68-7 Liquid Best Price

  • Molecular Formula:C9H9N
  • Molecular Weight:131.177
  • Appearance/Colour:clear colorless to orange-reddish liquid 
  • Vapor Pressure:4.52E-10mmHg at 25°C 
  • Melting Point:58 - 59oC 
  • Refractive Index:1.5264-1.5284  
  • Boiling Point:244 °C at 760 mmHg 
  • Flash Point:111.3 °C 
  • PSA:23.79000 
  • Density:0.994 g/cm3 
  • LogP:2.06108 

2-Methylbenzyl cyanide(Cas 22364-68-7) Usage

Chemical Properties

clear colorless to orange-reddish liquid

Uses

o-Tolylacetonitrile is used as an important raw material and intermediate in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is also used as an organic and chemical intermediate.

Definition

ChEBI: A nitrile that is acetonitrile where one of the methyl hydrogens is substituted by a 2-methylphenyl group.

Synthesis Reference(s)

Synthesis, p. 40, 1987 DOI: 10.1055/s-1987-27834

InChI:InChI=1/C7H12Cl2N2O2/c8-4-6(12)10-2-1-3-11-7(13)5-9/h1-5H2,(H,10,12)(H,11,13)

22364-68-7 Relevant articles

Influence of Functional Groups on the Ene Reaction of Singlet Oxygen with 1,4-Cyclohexadienes?

Fudickar, Werner,Metz, Melanie,Mai-Linde, Yasemin,Krüger, Tobias,Kelling, Alexandra,Sperlich, Eric,Linker, Torsten

, p. 1289 - 1297 (2021/05/13)

The photooxygenation of 1,4-cyclohexadie...

Reductive cyanation of organic chlorides using CO2 and NH3 via Triphos–Ni(I) species

Dong, Yanan,Li, Yuehui,Yang, Peiju,Zhao, Shizhen

, (2020/08/19)

Cyano-containing compounds constitute im...

Synthesis method of 3-isochromanone

-

, (2021/01/04)

The invention belongs to the technical f...

Titanium(III)-Catalyzed Reductive Decyanation of Geminal Dinitriles by a Non-Free-Radical Mechanism

Weweler, Jens,Younas, Sara L.,Streuff, Jan

, p. 17700 - 17703 (2019/11/13)

A titanium-catalyzed mono-decyanation of...

22364-68-7 Process route

C<sub>22</sub>H<sub>18</sub>N<sub>2</sub>O<sub>4</sub>
183657-67-2

C22H18N2O4

2-tolylmethylnitrile
22364-68-7

2-tolylmethylnitrile

biphenyl-4-carboxylic acid
92-92-2

biphenyl-4-carboxylic acid

Conditions
Conditions Yield
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In benzene; Heating;
96%
94%
chloroacetonitrile
107-14-2

chloroacetonitrile

toluene
108-88-3,15644-74-3,16713-13-6

toluene

butanedinitrile
110-61-2

butanedinitrile

3-methylbenzyl cyanide
2947-60-6

3-methylbenzyl cyanide

(4-methylphenyl)acetonitrile
2947-61-7

(4-methylphenyl)acetonitrile

1,1'-(1,2-ethanediyl)bisbenzene
103-29-7

1,1'-(1,2-ethanediyl)bisbenzene

dihydrocinnamonitrile
645-59-0

dihydrocinnamonitrile

2-tolylmethylnitrile
22364-68-7

2-tolylmethylnitrile

Conditions
Conditions Yield
In acetonitrile; Product distribution; Mechanism; Irradiation; different concentration ratios;
0.7%
6.4%
2.1%
In acetonitrile; for 22h; Kinetics; Product distribution; Mechanism; Irradiation;
6.4%
2.1%
0.7%

22364-68-7 Upstream products

  • 151-50-8
    151-50-8

    potassium cyanide

  • 89-92-9
    89-92-9

    2-methylbenzyl bromide

  • 143-33-9
    143-33-9

    sodium cyanide

  • 552-45-4
    552-45-4

    1-chloromethyl-2-methylbenzene

22364-68-7 Downstream products

  • 5466-19-3
    5466-19-3

    2-o-tolyl-pyrido[2,3-b]pyrazine-3,6-diyldiamine

  • 31881-09-1
    31881-09-1

    3c-(2-chloro-phenyl)-2-o-tolyl-acrylonitrile

  • 87968-36-3
    87968-36-3

    α-cyano-2-methylstilbene

  • 412282-12-3
    412282-12-3

    3-cyano-2-oxo-3-o-tolyl-propionic acid ethyl ester

Relevant Products