O-Ethyl 3-methylbenzene-1-carbothioate

Base Information

Chemical Name:O-Ethyl 3-methylbenzene-1-carbothioate
CAS No.:64559-07-5
Molecular Formula:C10H12OS
Molecular Weight:180.271
Hs Code.:
DSSTox Substance ID:DTXSID20510075
Nikkaji Number:J101.868J
Wikidata:Q82368119

Synonyms:64559-07-5;O-Ethyl 3-methylbenzene-1-carbothioate;DTXSID20510075

Suppliers and Price of O-Ethyl 3-methylbenzene-1-carbothioate

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of O-Ethyl 3-methylbenzene-1-carbothioate

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:180.06088618
Heavy Atom Count:12
Complexity:156

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of O-Ethyl 3-methylbenzene-1-carbothioate

There total 4 articles about O-Ethyl 3-methylbenzene-1-carbothioate 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: 87.0%

: 83247-16-9
2-Dimethylamino-2-ethoxy-2-(3-methylphenyl)acetonitril

: 64559-07-5
3-(Methyl)thiobenzoesaeure-O-ethylester

Guidance literature:: With hydrogen sulfide; In cyclohexane; at 70 - 80 ℃;

Reference yield:

: 6935-65-5
3,N,N-trimethylbenzamide

: 64559-07-5
3-(Methyl)thiobenzoesaeure-O-ethylester

Guidance literature:: Multi-step reaction with 3 steps

1: 12 h

2: H₂O; benzene / 0.08 h / 5 °C

3: 87 percent / H₂S / cyclohexane / 70 - 80 °C

With hydrogen sulfide; In cyclohexane; water; benzene;

Reference yield:

: C₁₂H₁₈NO⁽¹⁺⁾*BF₄^(1-)

: 64559-07-5
3-(Methyl)thiobenzoesaeure-O-ethylester

Guidance literature:: Multi-step reaction with 2 steps

1: H₂O; benzene / 0.08 h / 5 °C

2: 87 percent / H₂S / cyclohexane / 70 - 80 °C

With hydrogen sulfide; In cyclohexane; water; benzene;