Phenyl 2-mercaptobenzoate

Base Information

Chemical Name:Phenyl 2-mercaptobenzoate
CAS No.:15570-18-0
Molecular Formula:C13H10 O2 S
Molecular Weight:230.287
Hs Code.:
European Community (EC) Number:239-618-2
DSSTox Substance ID:DTXSID30165954
Nikkaji Number:J317.910I
Wikidata:Q83035210
Mol file:15570-18-0.mol

Synonyms:phenyl 2-sulfanylbenzoate;Phenyl 2-mercaptobenzoate;15570-18-0;EINECS 239-618-2;Benzoic acid, 2-mercapto-, phenyl ester;phenyl thiosalicylate;SCHEMBL943555;DTXSID30165954;2-Mercaptobenzoic acid phenyl ester

Suppliers and Price of Phenyl 2-mercaptobenzoate

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 4 raw suppliers

Chemical Property of Phenyl 2-mercaptobenzoate

Chemical Property:

Vapor Pressure:7.46E-06mmHg at 25°C
Boiling Point:376°C at 760 mmHg
Flash Point:279°C
PSA：65.10000
Density:1.241g/cm³
LogP:3.19450
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:230.04015073
Heavy Atom Count:16
Complexity:236

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OC(=O)C2=CC=CC=C2S

Technology Process of Phenyl 2-mercaptobenzoate

There total 2 articles about Phenyl 2-mercaptobenzoate 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: 76.0%

: 29585-74-8
diphenyl 2,2'-disulfanediyldibenzoate

: 15570-18-0
phenyl o-mercaptobenzoate

Guidance literature:: With hydrogenchloride; triphenylphosphine; In 1,4-dioxane; water; at 40 ℃; for 2h; Inert atmosphere;
DOI:10.1039/c6ob01758d

Reference yield: 60.0%

: 147-93-3
Thiosalicylic acid

: 108-95-2,27073-41-2
phenol

: 15570-18-0
phenyl o-mercaptobenzoate

Guidance literature:: With trichlorophosphate; at 135 ℃;
DOI:10.1039/c002480e

Reference yield: 95.0%

: 1206884-01-6
(E)-ethyl 3-(2-((E)-2-nitroprop-1-enyl)phenoxy)acrylate

: 15570-18-0
phenyl o-mercaptobenzoate

: ethyl 2-((2S,3S,4S)-3-methyl-3-nitro-4-(phenylthio)chroman-2-yl)acetate

: ethyl 2-((2R,3R,4R)-3-methyl-3-nitro-4-(phenylthio)chroman-2-yl)acetate

Guidance literature:: (E)-ethyl 3-(2-((E)-2-nitroprop-1-enyl)phenoxy)acrylate; With quinine; In acetonitrile; at 60 ℃; for 0.25h;

phenyl o-mercaptobenzoate; In acetonitrile; at 60 ℃; enantioselective reaction;
DOI:10.1021/ol400025a