(3-Amino-2,5-dimethylphenyl)acetonitrile

Base Information

Chemical Name:(3-Amino-2,5-dimethylphenyl)acetonitrile
CAS No.:57411-96-8
Molecular Formula:C10H12N2
Molecular Weight:160.2157
Hs Code.:
NSC Number:87680
DSSTox Substance ID:DTXSID90293186
Wikidata:Q82031824

Synonyms:57411-96-8;NSC 87680;(3-amino-2,5-dimethylphenyl)acetonitrile;NSC87680;DTXSID90293186;CCG-40518;NSC-87680

Suppliers and Price of (3-Amino-2,5-dimethylphenyl)acetonitrile

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of (3-Amino-2,5-dimethylphenyl)acetonitrile

Chemical Property:

Vapor Pressure:0.000212mmHg at 25°C
Boiling Point:326.7°Cat760mmHg
Flash Point:151.4°C
Density:1.064g/cm³
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:160.100048391
Heavy Atom Count:12
Complexity:191

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C(=C1)N)C)CC#N

Technology Process of (3-Amino-2,5-dimethylphenyl)acetonitrile

There total 2 articles about (3-Amino-2,5-dimethylphenyl)acetonitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 89-58-7
mononitro-p-xylene

: 57411-96-8
3-Cyanomethyl-2,5-dimethylanilin

Guidance literature:: Multi-step reaction with 2 steps

1: ClSO₃H, NaCl

2: (i) aq. EtOH, (ii) H₂, PtO₂, MeOH

With chlorosulfonic acid; sodium chloride;
DOI:10.1002/jhet.5570120322