3-Fluoro-4-(4-methylbenzene-1-sulfonyl)phenol

Base Information

Chemical Name:3-Fluoro-4-(4-methylbenzene-1-sulfonyl)phenol
CAS No.:87787-53-9
Molecular Formula:C13H11FO3S
Molecular Weight:266.293
Hs Code.:
DSSTox Substance ID:DTXSID90604233
Wikidata:Q82502056

Synonyms:3-Fluoro-4-(4-methylbenzene-1-sulfonyl)phenol;87787-53-9;SCHEMBL10967694;DTXSID90604233

Suppliers and Price of 3-Fluoro-4-(4-methylbenzene-1-sulfonyl)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

Total 1 raw suppliers

Chemical Property of 3-Fluoro-4-(4-methylbenzene-1-sulfonyl)phenol

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:266.04129354
Heavy Atom Count:18
Complexity:368

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)C2=C(C=C(C=C2)O)F

Technology Process of 3-Fluoro-4-(4-methylbenzene-1-sulfonyl)phenol

There total 3 articles about 3-Fluoro-4-(4-methylbenzene-1-sulfonyl)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:

: 372-20-3
3-fluorophenol

: 87787-53-9
3-fluoro-4-[(4-methylphenyl)sulfonyl]phenol

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / acetone; H₂O / 20 °C

2: graphite; MeSO₃H / 1 h / 120 °C

With methanesulfonic acid; potassium carbonate; pyrographite; In water; acetone; 2: thia-Fries rearrangement;
DOI:10.1002/hlca.200490295

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 87787-53-9
3-fluoro-4-[(4-methylphenyl)sulfonyl]phenol

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / acetone; H₂O / 20 °C

2: graphite; MeSO₃H / 1 h / 120 °C

With methanesulfonic acid; potassium carbonate; pyrographite; In water; acetone; 2: thia-Fries rearrangement;
DOI:10.1002/hlca.200490295