Ethyl 2-benzamido-2-cyclohexylideneacetate

Base Information

Chemical Name:Ethyl 2-benzamido-2-cyclohexylideneacetate
CAS No.:19642-36-5
Molecular Formula:C17H21NO3
Molecular Weight:287.359
Hs Code.:
DSSTox Substance ID:DTXSID00366916
ChEMBL ID:CHEMBL1880337

Synonyms:ethyl 2-benzamido-2-cyclohexylideneacetate;ethyl (benzoylamino)(cyclohexylidene)acetate;SMR000105037;CBMicro_036065;19642-36-5;MLS000109091;CHEMBL1880337;DTXSID00366916;HMS2284H23;BIM-0036013.P001;SR-01000466936;SR-01000466936-1

Suppliers and Price of Ethyl 2-benzamido-2-cyclohexylideneacetate

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
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price

Total 1 raw suppliers

Chemical Property of Ethyl 2-benzamido-2-cyclohexylideneacetate

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:287.15214353
Heavy Atom Count:21
Complexity:400

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)C(=C1CCCCC1)NC(=O)C2=CC=CC=C2

Technology Process of Ethyl 2-benzamido-2-cyclohexylideneacetate

There total 6 articles about Ethyl 2-benzamido-2-cyclohexylideneacetate 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: 86.0%

: 64-17-5
ethanol

: 52956-46-4
4-cyclohexylidene-2-phenyloxazol-5(4H)-one

: 19642-36-5
ethyl 1-(N-benzoylamino)-1-cyclohexylideneacetate

Guidance literature:: With triethylamine; for 3h; Heating;

Reference yield: 15.0%

: 13275-31-5
ethyl cyclohexyloxoacetate

: 55-21-0,27208-38-4
benzamide

: 19642-36-5
ethyl 1-(N-benzoylamino)-1-cyclohexylideneacetate

Guidance literature:: With trichlorophosphate; In benzene; for 12h; Heating;

Reference yield:

: 931-50-0
cyclohexylmagnesium bromide

: 19642-36-5
ethyl 1-(N-benzoylamino)-1-cyclohexylideneacetate

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether / 2 h / -10 °C

2: 15 percent / phosphoryl chloride / benzene / 12 h / Heating

With trichlorophosphate; In diethyl ether; benzene;