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

Base Information

Chemical Name:N-(2-cyclopentylbenzotriazol-5-yl)-4-methylbenzenesulfonamide
CAS No.:130787-22-3
Molecular Formula:C₁₈H₂₀N₄O₂S
Molecular Weight:356.448
Hs Code.:
DSSTox Substance ID:DTXSID30872232
Nikkaji Number:J1.564.265C

Synonyms:130787-22-3;DTXSID30872232;N-(2-Cyclopentyl-2H-benzotriazol-5-yl)-4-methylbenzene-1-sulfonamide

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

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-methylbenzenesulfonamide

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:356.13069707
Heavy Atom Count:25
Complexity:550

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)NC2=CC3=NN(N=C3C=C2)C4CCCC4

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

There total 4 articles about N-(2-cyclopentylbenzotriazol-5-yl)-4-methylbenzenesulfonamide 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: 31.0%

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

: 98-59-9
p-toluenesulfonyl chloride

: 130787-22-3
N-(2-Cyclopentyl-2H-benzotriazol-5-yl)-4-methyl-benzenesulfonamide

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

Reference yield:

: 137-43-9
Cyclopentyl bromide

: 130787-22-3
N-(2-Cyclopentyl-2H-benzotriazol-5-yl)-4-methyl-benzenesulfonamide

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: 31 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

: 130787-22-3
N-(2-Cyclopentyl-2H-benzotriazol-5-yl)-4-methyl-benzenesulfonamide

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: 31 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