2,2-dichloro-N-(2-cyclohexylbenzotriazol-5-yl)acetamide

Base Information

Chemical Name:2,2-dichloro-N-(2-cyclohexylbenzotriazol-5-yl)acetamide
CAS No.:142312-58-1
Molecular Formula:C₁₄H₁₆Cl₂N₄O
Molecular Weight:327.213
Hs Code.:
DSSTox Substance ID:DTXSID10872250
Nikkaji Number:J483.152G

Synonyms:142312-58-1;2,2-dichloro-N-(2-cyclohexylbenzotriazol-5-yl)acetamide;DTXSID10872250;2-Cyclohexyl-5-(dichloroacetyl)amino-2H-benzotriazole;2,2-Dichloro-N-(2-cyclohexyl-2H-benzotriazol-5-yl)acetamide;Acetamide, 2,2-dichloro-N-(2-cyclohexyl-2H-1,2,3-benzotriazol-5-yl)-

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

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Chemical Property of 2,2-dichloro-N-(2-cyclohexylbenzotriazol-5-yl)acetamide

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:326.0701165
Heavy Atom Count:21
Complexity:376

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(CC1)N2N=C3C=CC(=CC3=N2)NC(=O)C(Cl)Cl

Technology Process of 2,2-dichloro-N-(2-cyclohexylbenzotriazol-5-yl)acetamide

There total 4 articles about 2,2-dichloro-N-(2-cyclohexylbenzotriazol-5-yl)acetamide 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: 47.0%

: 79-36-7
dichloroacethyl chloride

: 142312-69-4
2-cyclohexyl-5-aminobenzotriazole

: 142312-58-1
2,2-Dichloro-N-(2-cyclohexyl-2H-benzotriazol-5-yl)-acetamide

Guidance literature:: With pyridine; In benzene; for 4h; Heating;
DOI:10.1016/0223-5234(92)90105-A

Reference yield:

: 108-85-0
1-bromocyclohexane

: 142312-58-1
2,2-Dichloro-N-(2-cyclohexyl-2H-benzotriazol-5-yl)-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 38 percent / EtONa / ethanol / 72 h / Heating

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

3: 47 percent / pyridine / benzene / 4 h / Heating

With pyridine; hydrogen; sodium ethanolate; palladium on activated charcoal; In methanol; ethanol; benzene;
DOI:10.1016/0223-5234(92)90105-A

Reference yield:

: 2338-12-7
5-nitrobenzotriazole

: 142312-58-1
2,2-Dichloro-N-(2-cyclohexyl-2H-benzotriazol-5-yl)-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 38 percent / EtONa / ethanol / 72 h / Heating

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

3: 47 percent / pyridine / benzene / 4 h / Heating

With pyridine; hydrogen; sodium ethanolate; palladium on activated charcoal; In methanol; ethanol; benzene;
DOI:10.1016/0223-5234(92)90105-A