Benzamide, N-(cyclohexylcarbonyl)-

Base Information

Chemical Name:Benzamide, N-(cyclohexylcarbonyl)-
CAS No.:1738-55-2
Molecular Formula:C14H17NO2
Molecular Weight:231.294
Hs Code.:
DSSTox Substance ID:DTXSID30406692
Wikidata:Q82211778

Synonyms:Benzamide, N-(cyclohexylcarbonyl)-;N-(cyclohexanecarbonyl)benzamide;1738-55-2;SCHEMBL4266412;DTXSID30406692;AKOS030579116;SR-01000061859;SR-01000061859-1;Z57055823

Suppliers and Price of Benzamide, N-(cyclohexylcarbonyl)-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of Benzamide, N-(cyclohexylcarbonyl)-

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:231.125928785
Heavy Atom Count:17
Complexity:276

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(CC1)C(=O)NC(=O)C2=CC=CC=C2

Technology Process of Benzamide, N-(cyclohexylcarbonyl)-

There total 5 articles about Benzamide, N-(cyclohexylcarbonyl)- 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: 91.0%

: 917988-90-0
2-cyclohexyl-4,5-diphenyloxazole

: 1738-55-2
N-(cyclohexanecarbonyl)benzamide

Guidance literature:: With ammonium cerium(IV) nitrate; water; In acetonitrile; at 20 ℃; for 2h;
DOI:10.1021/ol0624530

Reference yield: 91.0%

: 35665-26-0
N-benzylcyclohexanecarboxamide

: 1738-55-2
N-(cyclohexanecarbonyl)benzamide

Guidance literature:: With acetic anhydride; periodic acid; chromium(VI) oxide; In acetonitrile; at 0 ℃;
DOI:10.1039/b404823g

Reference yield:

: 50889-12-8
2-oxo-1,2-diphenylethyl cyclohexanecarboxylate

: 1738-55-2
N-(cyclohexanecarbonyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / ammonium acetate; acetic acid / 2 h / Heating

2: 91 percent / ceric ammonium nitrate; water / acetonitrile / 2 h / 20 °C

With ammonium acetate; ammonium cerium(IV) nitrate; water; acetic acid; In acetonitrile;
DOI:10.1021/ol0624530