Benzenecarbodithioic acid, 2,3,4-trihydroxy- (9CI)

Base Information

Chemical Name:Benzenecarbodithioic acid, 2,3,4-trihydroxy- (9CI)
CAS No.:32361-59-4
Molecular Formula:C7H6 O3 S2
Molecular Weight:202.255
Hs Code.:2930909090
Mol file:32361-59-4.mol

Synonyms:Benzoicacid, 2,3,4-trihydroxydithio- (8CI); 2,3,4-Trihydroxydithiobenzoic acid

Suppliers and Price of Benzenecarbodithioic acid, 2,3,4-trihydroxy- (9CI)

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 Benzenecarbodithioic acid, 2,3,4-trihydroxy- (9CI)

Chemical Property:

PSA：135.13000
LogP:1.52410

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Benzenecarbodithioic acid, 2,3,4-trihydroxy- (9CI)

There total 1 articles about Benzenecarbodithioic acid, 2,3,4-trihydroxy- (9CI) 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:

: 140-89-6
potassium ethyl xanthogenate

: 87-66-1
2-hydroxyresorcinol

: 32361-59-4
2,3,4-trihydroxy-dithiobenzoic acid

Guidance literature:: With ethanol; at 100 ℃;
DOI:10.1007/BF01516465

Reference yield:

: 32361-59-4
2,3,4-trihydroxy-dithiobenzoic acid

: 610-02-6
2,3,4-trihydroxybenzoic acid

Guidance literature:: DOI:10.1007/BF01516465

Reference yield:

: 32361-59-4
2,3,4-trihydroxy-dithiobenzoic acid

: 1357359-23-9
4-(1,3-thiazolo[5,4-b]pyridin-2-yl)benzene-1,2,3-triol

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride

2: methanol / 3 h / Reflux

With thionyl chloride; In methanol;
DOI:10.1002/cbdv.201100007