3-(Trifluoromethylthio)phenol

Base Information

Chemical Name:3-(Trifluoromethylthio)phenol
CAS No.:3823-40-3
Molecular Formula:C7H5F3OS
Molecular Weight:194.177
Hs Code.:2930909090
DSSTox Substance ID:DTXSID70380700
Wikidata:Q82171107
Mol file:3823-40-3.mol

Synonyms:3-(Trifluoromethylthio)phenol;3823-40-3;3-(trifluoromethylsulfanyl)phenol;3-[(trifluoromethyl)thio]phenol;3-((Trifluoromethyl)thio)phenol;3-(trifluoromethylthio) phenol;3-[(trifluoromethyl)sulfanyl]phenol;SCHEMBL514189;DTXSID70380700;MFCD06248888;AKOS024348843;AS-33045;CS-0107249;FT-0614815;EN300-1928916;A824074

Suppliers and Price of 3-(Trifluoromethylthio)phenol

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

TRC
3-[(Trifluoromethyl)thio]phenol
50mg
$ 165.00

Labseeker
3-(TRIFLUOROMETHYLTHIO)PHENOL 95
1g
$ 599.00

Crysdot
3-[(Trifluoromethyl)thio]phenol 95+%
5g
$ 736.00

American Custom Chemicals Corporation
3-(TRIFLUOROMETHYLTHIO)PHENOL 95.00%
25G
$ 1574.15

Alichem
3-(Trifluoromethylthio)phenol
1g
$ 1579.40

Alichem
3-(Trifluoromethylthio)phenol
250mg
$ 489.60

Total 19 raw suppliers

Chemical Property of 3-(Trifluoromethylthio)phenol

Chemical Property:

Vapor Pressure:1.38mmHg at 25°C
Melting Point:67-68°C
Boiling Point:76-80°C 2,5mm
Flash Point:54.2°C
PSA：45.53000
Density:1.45g/cm³
LogP:3.00410
Sensitive.:Stench
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:194.00132044
Heavy Atom Count:12
Complexity:148

Purity/Quality:

95% ^*data from raw suppliers

3-[(Trifluoromethyl)thio]phenol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 20/21/22-36/37/38
Safety Statements: 26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)SC(F)(F)F)O
Uses 3-[(Trifluoromethyl)thio]phenol is a reactant used in the preparation of 2-azolyl-4-phenoxypyrimidines as highly active herbicides that inhibit carotenoid biosynthesis.

Technology Process of 3-(Trifluoromethylthio)phenol

There total 3 articles about 3-(Trifluoromethylthio)phenol 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: 92.0%

: 626-02-8
3-Iodophenol

: 811-68-7
silver(I) trifluoromethanethiolate

: 3823-40-3
3-(trifluoromethylthio) phenol

Guidance literature:: With silver hexafluoroantimonate; chloro[di(1-adamantyl)-2-dimethylaminophenylphosphine]gold(I); In 1,2-dichloro-ethane; at 70 ℃; for 1h;
DOI:10.1002/anie.202115687

Reference yield:

: 369-68-6
3-(trifluoromethylthio)aniline

: 3823-40-3
3-(trifluoromethylthio) phenol

Guidance literature:: Multistep reaction; (i) (diazotization), (ii) (hydrolysis);
DOI:10.1021/jo01027a033

Reference yield:

: 3823-40-3
3-(trifluoromethylthio) phenol

Guidance literature:: 3-Trifluormethylmercapto-anilin, 1. wss. NaNO2-Lsg., H2SO4, 0grad (-> Diazoniumsalz), 2. H2SO4, Erh.;
DOI:10.1021/ja00901a033