(1-Ethyl-1H-1,2,3-triazol-4-yl)phenylmethanone

Base Information

Chemical Name:(1-Ethyl-1H-1,2,3-triazol-4-yl)phenylmethanone
CAS No.:134926-96-8
Molecular Formula:C₁₁H₁₁N₃O
Molecular Weight:201.228
Hs Code.:
DSSTox Substance ID:DTXSID101246012

Synonyms:(1-Ethyl-1H-1,2,3-triazol-4-yl)phenylmethanone;DTXSID101246012;134926-96-8;(1-ethyl-1h-[1,2,3]triazol-4-yl)-phenyl-methanone

Suppliers and Price of (1-Ethyl-1H-1,2,3-triazol-4-yl)phenylmethanone

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 0 raw suppliers

Chemical Property of (1-Ethyl-1H-1,2,3-triazol-4-yl)phenylmethanone

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:201.090211983
Heavy Atom Count:15
Complexity:226

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCN1C=C(N=N1)C(=O)C2=CC=CC=C2

Technology Process of (1-Ethyl-1H-1,2,3-triazol-4-yl)phenylmethanone

There total 4 articles about (1-Ethyl-1H-1,2,3-triazol-4-yl)phenylmethanone 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: 42.0%

: 75-04-7,85404-22-4
ethylamine

: 151918-49-9
5-phenyl-1,2,3-thiadiazole-4-carbaldehyde

: 134926-96-8
4-benzoyl-1-ethyl-1,2,3-triazole

Guidance literature:: In ethanol; for 24h; Ambient temperature;

Reference yield:

: 18212-29-8
5-phenyl-1,2,3-thiadiazole

: 134926-96-8
4-benzoyl-1-ethyl-1,2,3-triazole

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / MeLi / tetrahydrofuran; diethyl ether / 1.) -78 deg C, 1 h, 2.) -70 deg C, 1 h; room temperature, 12 h

2: 42 percent / ethanol / 24 h / Ambient temperature

With methyllithium; In tetrahydrofuran; diethyl ether; ethanol;

Reference yield:

: 79866-78-7
1,5-diphenyl-1H-1,2,3-triazole-4-carbaldehyde

: 134926-96-8
4-benzoyl-1-ethyl-1,2,3-triazole

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / ethanol; H₂O / Ambient temperature

2: 2) silica gel / 1) xylene, heating, 2) silica gel, chloroform

With silica gel; In ethanol; water;