1H-1,2,4-Triazole, 3-[4-(chloromethyl)phenyl]-1-ethyl-5-methyl-

Base Information

Chemical Name:1H-1,2,4-Triazole, 3-[4-(chloromethyl)phenyl]-1-ethyl-5-methyl-
CAS No.:511541-23-4
Molecular Formula:C12H14ClN3
Molecular Weight:235.716
Hs Code.:
DSSTox Substance ID:DTXSID90475940
Wikidata:Q82306775

Synonyms:511541-23-4;1H-1,2,4-Triazole, 3-[4-(chloromethyl)phenyl]-1-ethyl-5-methyl-;DTXSID90475940

Suppliers and Price of 1H-1,2,4-Triazole, 3-[4-(chloromethyl)phenyl]-1-ethyl-5-methyl-

Supply Marketing:

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

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Chemical Property of 1H-1,2,4-Triazole, 3-[4-(chloromethyl)phenyl]-1-ethyl-5-methyl-

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:235.0876252
Heavy Atom Count:16
Complexity:216

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN1C(=NC(=N1)C2=CC=C(C=C2)CCl)C

Technology Process of 1H-1,2,4-Triazole, 3-[4-(chloromethyl)phenyl]-1-ethyl-5-methyl-

There total 1 articles about 1H-1,2,4-Triazole, 3-[4-(chloromethyl)phenyl]-1-ethyl-5-methyl- 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: 80.0%

: 52406-48-1
α,α'-dichloroazo compound

: 874-86-2
4-cyanobenzyl chloride

: 511541-23-4
1-ethyl-5-methyl-3-[4-chlorobenzyl-1-yl]-1H-1,2,4-triazole

Guidance literature:: α,α'-dichloroazo compound; 4-cyanobenzyl chloride; With antimonypentachloride; In dichloromethane; at -60 - 23 ℃; for 2.16667h;

With ammonium hydroxide; sodium hydrogencarbonate; In acetonitrile; at 0 - 20 ℃;
DOI:10.1080/00304940209355790