3,4-dichloro-N-(2-cyclopentylbenzotriazol-5-yl)benzamide

Base Information

Chemical Name:3,4-dichloro-N-(2-cyclopentylbenzotriazol-5-yl)benzamide
CAS No.:130787-19-8
Molecular Formula:C₁₈H₁₆Cl₂N₄O
Molecular Weight:375.257
Hs Code.:
DSSTox Substance ID:DTXSID00872229
Nikkaji Number:J1.564.193B

Synonyms:130787-19-8;DTXSID00872229;3,4-Dichloro-N-(2-cyclopentyl-2H-benzotriazol-5-yl)benzamide

Suppliers and Price of 3,4-dichloro-N-(2-cyclopentylbenzotriazol-5-yl)benzamide

Supply Marketing:

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

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Chemical Property of 3,4-dichloro-N-(2-cyclopentylbenzotriazol-5-yl)benzamide

Chemical Property:

XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:374.0701165
Heavy Atom Count:25
Complexity:488

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(C1)N2N=C3C=CC(=CC3=N2)NC(=O)C4=CC(=C(C=C4)Cl)Cl

Technology Process of 3,4-dichloro-N-(2-cyclopentylbenzotriazol-5-yl)benzamide

There total 4 articles about 3,4-dichloro-N-(2-cyclopentylbenzotriazol-5-yl)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: 50.0%

: 130787-05-2
2-cyclopentyl-5-aminobenzotriazole

: 3024-72-4
3,4-dichlorobenzoyl chloride

: 130787-19-8
3,4-Dichloro-N-(2-cyclopentyl-2H-benzotriazol-5-yl)-benzamide

Guidance literature:: With pyridine; In benzene; for 4h; Heating;
DOI:10.1016/0223-5234(90)90118-M

Reference yield:

: 137-43-9
Cyclopentyl bromide

: 130787-19-8
3,4-Dichloro-N-(2-cyclopentyl-2H-benzotriazol-5-yl)-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 38 percent / C₂H₅ONa / 24 h / Heating

2: 100 percent / H₂ / 10percent Pd/C / methanol / Ambient temperature

3: 50 percent / pyridine / benzene / 4 h / Heating

With pyridine; hydrogen; sodium ethanolate; palladium on activated charcoal; In methanol; benzene;
DOI:10.1016/0223-5234(90)90118-M

Reference yield:

: 2338-12-7
5-nitrobenzotriazole

: 130787-19-8
3,4-Dichloro-N-(2-cyclopentyl-2H-benzotriazol-5-yl)-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 38 percent / C₂H₅ONa / 24 h / Heating

2: 100 percent / H₂ / 10percent Pd/C / methanol / Ambient temperature

3: 50 percent / pyridine / benzene / 4 h / Heating

With pyridine; hydrogen; sodium ethanolate; palladium on activated charcoal; In methanol; benzene;
DOI:10.1016/0223-5234(90)90118-M