Benzenecarbothioic acid, S-cyclohexyl ester

Base Information

Chemical Name:Benzenecarbothioic acid, S-cyclohexyl ester
CAS No.:10035-90-2
Molecular Formula:C13H16OS
Molecular Weight:220.335
Hs Code.:
DSSTox Substance ID:DTXSID80457619
Nikkaji Number:J1.432.375I
Wikidata:Q82280529
Mol file:10035-90-2.mol

Synonyms:Benzenecarbothioic acid, S-cyclohexyl ester;10035-90-2;S-Cyclohexyl benzothioate;S-cyclohexyl benzenecarbothioate;SCHEMBL6057177;DTXSID80457619;Thiobenzoic acid S-cyclohexyl ester

Suppliers and Price of Benzenecarbothioic acid, S-cyclohexyl ester

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 Benzenecarbothioic acid, S-cyclohexyl ester

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:220.09218630
Heavy Atom Count:15
Complexity:203

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(CC1)SC(=O)C2=CC=CC=C2

Technology Process of Benzenecarbothioic acid, S-cyclohexyl ester

There total 18 articles about Benzenecarbothioic acid, S-cyclohexyl ester 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: 97.0%

: 1569-69-3
Cyclohexanethiol

: 98-88-4
benzoyl chloride

: 10035-90-2
S-cyclohexyl benzothioate

Guidance literature:: With 1,1,1,3',3',3'-hexafluoro-propanol; In neat (no solvent); at 20 ℃; for 0.0166667h; Green chemistry;
DOI:10.1016/j.tetlet.2017.04.004