N-(2-cyclopentylbenzotriazol-5-yl)-4-nitrobenzamide

Base Information

Chemical Name:N-(2-cyclopentylbenzotriazol-5-yl)-4-nitrobenzamide
CAS No.:130787-18-7
Molecular Formula:C₁₈H₁₇N₅O₃
Molecular Weight:351.365
Hs Code.:
DSSTox Substance ID:DTXSID40872228
Nikkaji Number:J1.564.192D

Synonyms:130787-18-7;DTXSID40872228;N-(2-Cyclopentyl-2H-benzotriazol-5-yl)-4-nitrobenzamide

Suppliers and Price of N-(2-cyclopentylbenzotriazol-5-yl)-4-nitrobenzamide

Supply Marketing:

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

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Chemical Property of N-(2-cyclopentylbenzotriazol-5-yl)-4-nitrobenzamide

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:351.13313942
Heavy Atom Count:26
Complexity:525

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)[N+](=O)[O-]

Technology Process of N-(2-cyclopentylbenzotriazol-5-yl)-4-nitrobenzamide

There total 4 articles about N-(2-cyclopentylbenzotriazol-5-yl)-4-nitrobenzamide 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: 32.0%

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

: 122-04-3
4-nitro-benzoyl chloride

: 130787-18-7
N-(2-Cyclopentyl-2H-benzotriazol-5-yl)-4-nitro-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

: 130787-18-7
N-(2-Cyclopentyl-2H-benzotriazol-5-yl)-4-nitro-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: 32 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

: 130787-18-7
N-(2-Cyclopentyl-2H-benzotriazol-5-yl)-4-nitro-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: 32 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