N-(4-(2-Ethyl-2H-1,2,3-triazol-4-yl)phenyl)benzamide

Base Information

Chemical Name:N-(4-(2-Ethyl-2H-1,2,3-triazol-4-yl)phenyl)benzamide
CAS No.:89221-06-7
Molecular Formula:C₁₇H₁₆N₄O
Molecular Weight:292.34
Hs Code.:
DSSTox Substance ID:DTXSID00539421
Wikidata:Q82415164

Synonyms:89221-06-7;N-(4-(2-Ethyl-2H-1,2,3-triazol-4-yl)phenyl)benzamide;N-[4-(2-Ethyl-2H-1,2,3-triazol-4-yl)phenyl]benzamide;DTXSID00539421

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

Supply Marketing:

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

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Chemical Property of N-(4-(2-Ethyl-2H-1,2,3-triazol-4-yl)phenyl)benzamide

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:292.13241115
Heavy Atom Count:22
Complexity:362

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN1N=CC(=N1)C2=CC=C(C=C2)NC(=O)C3=CC=CC=C3

Technology Process of N-(4-(2-Ethyl-2H-1,2,3-triazol-4-yl)phenyl)benzamide

There total 5 articles about N-(4-(2-Ethyl-2H-1,2,3-triazol-4-yl)phenyl)benzamide 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%

: 98-88-4
benzoyl chloride

: 89220-94-0
2-ethyl-4-(4-aminophenyl)-1,2,3-triazole

: 89221-06-7
2-ethyl-4-<4-(N-benzoylamino)phenyl>-1,2,3-triazole

Guidance literature:: at 70 ℃; for 12h;

Reference yield:

: 89220-93-9
2-ethyl-4-(4-nitrophenyl)-1,2,3-triazole

: 89221-06-7
2-ethyl-4-<4-(N-benzoylamino)phenyl>-1,2,3-triazole

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / 85percent hydrazine hydrate / 10percent Pd/C / ethanol / 50 °C

2: 80 percent / 12 h / 70 °C

With hydrazine hydrate; palladium on activated charcoal; In ethanol;

Reference yield:

: 6111-97-3
5-(4-nitrophenyl)-1H-1,2,3-triazole

: 89221-06-7
2-ethyl-4-<4-(N-benzoylamino)phenyl>-1,2,3-triazole

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / sodium methoxide / methanol / 24 h / Heating

2: 90 percent / 85percent hydrazine hydrate / 10percent Pd/C / ethanol / 50 °C

3: 80 percent / 12 h / 70 °C

With sodium methylate; hydrazine hydrate; palladium on activated charcoal; In methanol; ethanol;