Benzenecarbothioic acid, 4-methoxy-, O-ethyl ester

Base Information

Chemical Name:Benzenecarbothioic acid, 4-methoxy-, O-ethyl ester
CAS No.:10602-66-1
Molecular Formula:C10H12O2S
Molecular Weight:196.27
Hs Code.:2930909090
DSSTox Substance ID:DTXSID60446809
Nikkaji Number:J102.196F
Mol file:10602-66-1.mol

Synonyms:10602-66-1;Benzenecarbothioic acid, 4-methoxy-, O-ethyl ester;O-ethyl 4-methoxybenzenecarbothioate;4-Methoxythiobenzoic acid ethyl ester;DTXSID60446809;p-Anisic acid, thio-, O-ethyl ester;4-Methoxy-thiobenzoic acid O-ethyl ester

Suppliers and Price of Benzenecarbothioic acid, 4-methoxy-, O-ethyl 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 3 raw suppliers

Chemical Property of Benzenecarbothioic acid, 4-methoxy-, O-ethyl ester

Chemical Property:

PSA：50.55000
LogP:2.40720
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:196.05580079
Heavy Atom Count:13
Complexity:162

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=S)C1=CC=C(C=C1)OC

Technology Process of Benzenecarbothioic acid, 4-methoxy-, O-ethyl ester

There total 8 articles about Benzenecarbothioic acid, 4-methoxy-, O-ethyl 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: 100.0%

: 829-48-1
4-methoxy-benzimidic acid ethyl ester

: 10602-66-1
O-ethyl 4-methoxythiobenzoate

Guidance literature:: With Dowex 50W-X₈; hydrogen sulfide; In methanol; at -20 ℃; for 1h;
DOI:10.1055/s-1989-27288

Reference yield: 73.0%

: 5-(4-Methoxy-phenyl)-[1,4,2]dithiazol-1-ylium; perchlorate

: 10602-66-1
O-ethyl 4-methoxythiobenzoate

Guidance literature:: With sodium ethanolate; In ethanol; for 0.333333h;

Reference yield:

: 874-90-8
4-methoxybenzonitrile

: 10602-66-1
O-ethyl 4-methoxythiobenzoate

Guidance literature:: Multi-step reaction with 2 steps

1: HCl / CHCl₃ / 120 h / 0 °C

2: 100 percent / H₂S, Dowex 50W-X₈ / methanol / 1 h / -20 °C

With hydrogenchloride; Dowex 50W-X₈; hydrogen sulfide; In methanol; chloroform;
DOI:10.1055/s-1989-27288