N-Cyclohexyl-4-methylbenzamide

Base Information

Chemical Name:N-Cyclohexyl-4-methylbenzamide
CAS No.:53205-68-8
Molecular Formula:C14H19 N O
Molecular Weight:217.311
Hs Code.:2924299090
NSC Number:21781
DSSTox Substance ID:DTXSID40281477
Nikkaji Number:J2.209.118B
Wikidata:Q82015434
ChEMBL ID:CHEMBL1410388
Mol file:53205-68-8.mol

Synonyms:N-Cyclohexyl-4-methylbenzamide;53205-68-8;N-CYCLOHEXYL-4-METHYL-BENZAMIDE;NSC21781;MLS000518966;SCHEMBL178426;N-cyclohexyl4-methyl benzamide;F0722-3774;CHEMBL1410388;DTXSID40281477;HMS2488C23;MFCD00453780;NSC 21781;NSC-21781;STL293557;AKOS001605241;SMR000129386;EU-0069668;AB00489800-08;SR-01000414971;SR-01000414971-1

Suppliers and Price of N-Cyclohexyl-4-methylbenzamide

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

Aronis compounds
N-cyclohexyl-4-methylbenzamide
50mg
$ 50.00

Aronis compounds
N-cyclohexyl-4-methylbenzamide
5mg
$ 15.00

American Custom Chemicals Corporation
N-CYCLOHEXYL-4-METHYL-BENZAMIDE 95.00%
5MG
$ 503.87

Total 4 raw suppliers

Chemical Property of N-Cyclohexyl-4-methylbenzamide

Chemical Property:

Vapor Pressure:4.85E-06mmHg at 25°C
Boiling Point:382.1°Cat760mmHg
Flash Point:230.4°C
PSA：29.10000
Density:1.04g/cm³
LogP:3.44840
XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:217.146664230
Heavy Atom Count:16
Complexity:225

Purity/Quality:

99% ^*data from raw suppliers

N-cyclohexyl-4-methylbenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(=O)NC2CCCCC2

Technology Process of N-Cyclohexyl-4-methylbenzamide

There total 37 articles about N-Cyclohexyl-4-methylbenzamide 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: 96.0%

: 108-91-8,157973-60-9
cyclohexylamine

: 99-94-5
p-Toluic acid

: 53205-68-8
N-cyclohexyl-p-toluamide

Guidance literature:: With (3-{[(cyclohexylimino)methylidene]amino}propyl)oxy linked polystyrene resin; In dichloromethane; N,N-dimethyl-formamide; for 0.0833333h; Flow reactor;
DOI:10.1021/acscombsci.0c00001

Reference yield: 93.0%

: 106-38-7
para-bromotoluene

: C₈H₁₂NO₃^(1-)*K⁽¹⁺⁾

: 53205-68-8
N-cyclohexyl-p-toluamide

Guidance literature:: With bis(benzonitrile)palladium(ll) chloride; [4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis{3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC}iridium(III) hexafluorophosphate; sodium acetate; nixantphos; In N,N-dimethyl acetamide; at 25 ℃; for 20h; chemoselective reaction; Schlenk technique; Inert atmosphere; Irradiation;
DOI:10.1002/chem.201502286

Reference yield: 92.0%

: 108-91-8,157973-60-9
cyclohexylamine

: 619-55-6
para-methylbenzamide

: 53205-68-8
N-cyclohexyl-p-toluamide

Guidance literature:: With C₂₈H₂₆ClN₃ORuS; In 1,4-dioxane; at 100 ℃; for 8h; Sealed tube; Inert atmosphere;
DOI:10.1016/j.jorganchem.2020.121555