1H-1,2,3-Triazole, 4-methyl-1-phenyl-

Base Information

Chemical Name:1H-1,2,3-Triazole, 4-methyl-1-phenyl-
CAS No.:20320-20-1
Molecular Formula:C9H9 N3
Molecular Weight:159.191
Hs Code.:
NSC Number:133516
DSSTox Substance ID:DTXSID50299886
Nikkaji Number:J408.391A
Wikidata:Q82042580

Synonyms:20320-20-1;1H-1,2,3-Triazole, 4-methyl-1-phenyl-;NSC133516;SCHEMBL2629357;DTXSID50299886;NSC-133516;1H-1,3-Triazole, 4-methyl-1-phenyl-

Suppliers and Price of 1H-1,2,3-Triazole, 4-methyl-1-phenyl-

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 5 raw suppliers

Chemical Property of 1H-1,2,3-Triazole, 4-methyl-1-phenyl-

Chemical Property:

Vapor Pressure:0.00131mmHg at 25°C
Boiling Point:297.9°Cat760mmHg
Flash Point:134°C
Density:1.13g/cm³
XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:159.079647300
Heavy Atom Count:12
Complexity:143

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CN(N=N1)C2=CC=CC=C2

Technology Process of 1H-1,2,3-Triazole, 4-methyl-1-phenyl-

There total 13 articles about 1H-1,2,3-Triazole, 4-methyl-1-phenyl- 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: 99.0%

: 123-38-6
propionaldehyde

: 622-37-7
Phenyl azide

: 20320-20-1
4-benzyl-1-(4-fluorophenyl)-1H-1,2,3-triazole

Guidance literature:: propionaldehyde; Phenyl azide; With pyrrolidine; In tetrahydrofuran; at 50 ℃; for 12h;

With 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; at 0 - 20 ℃; for 1h; Reagent/catalyst; Solvent; Temperature; regioselective reaction;
DOI:10.1002/ejoc.201500360

Reference yield: 97.0%

: 62-53-3
aniline

: 91257-99-7
N′-(2,2-dichloro-1-methylethylidene)-4-methylbenzenesulfonohydrazide

: 20320-20-1
4-benzyl-1-(4-fluorophenyl)-1H-1,2,3-triazole

Guidance literature:: aniline; With N-ethyl-N,N-diisopropylamine; In ethanol; at 0 ℃; for 0.166667h;

N′-(2,2-dichloro-1-methylethylidene)-4-methylbenzenesulfonohydrazide; In ethanol; acetonitrile; at 0 - 20 ℃; for 16h; chemoselective reaction;
DOI:10.1002/anie.201108850

Reference yield: 95.0%

: 591-50-4
iodobenzene

: 590-93-2
2-Butynoic acid

: 20320-20-1
4-benzyl-1-(4-fluorophenyl)-1H-1,2,3-triazole

Guidance literature:: With sodium azide; copper(ll) sulfate pentahydrate; sodium 2-(1,2-dihydroxyethyl)-4-hydroxy-5-oxo-2,5-dihydro-furan-3-olate; potassium carbonate; L-proline; In water; dimethyl sulfoxide; at 65 ℃;
DOI:10.1021/jo1024927