N-(2-Iodophenyl)benzenecarbothioamide

Base Information

Chemical Name:N-(2-Iodophenyl)benzenecarbothioamide
CAS No.:85445-09-6
Molecular Formula:C13H10INS
Molecular Weight:339.2
Hs Code.:
DSSTox Substance ID:DTXSID30515470
Wikidata:Q82376364

Synonyms:N-(2-Iodophenyl)benzenecarbothioamide;85445-09-6;N-(2-Iodophenyl)benzothioamide;N-(2-iodophenyl)-benzothioamide;DTXSID30515470;A904479

Suppliers and Price of N-(2-Iodophenyl)benzenecarbothioamide

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 9 raw suppliers

Chemical Property of N-(2-Iodophenyl)benzenecarbothioamide

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:338.95787
Heavy Atom Count:16
Complexity:238

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=S)NC2=CC=CC=C2I

Technology Process of N-(2-Iodophenyl)benzenecarbothioamide

There total 3 articles about N-(2-Iodophenyl)benzenecarbothioamide 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: 56.0%

: 15310-02-8
o-iodobenzanilide

: 85445-09-6
N-(2-iodophenyl)benzothioamide

Guidance literature:: With Lawessons reagent; In toluene; for 4h; Heating;
DOI:10.1016/S0040-4020(01)96061-2

Reference yield:

: 615-43-0
2-iodophenylamine

: 85445-09-6
N-(2-iodophenyl)benzothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / 10percent aq. NaOH / 2 h

2: 56 percent / Lawesson's reagent / toluene / 4 h / Heating

With Lawessons reagent; sodium hydroxide; In toluene;
DOI:10.1016/S0040-4020(01)96061-2

Reference yield:

: 98-88-4
benzoyl chloride

: 85445-09-6
N-(2-iodophenyl)benzothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / 10percent aq. NaOH / 2 h

2: 56 percent / Lawesson's reagent / toluene / 4 h / Heating

With Lawessons reagent; sodium hydroxide; In toluene;
DOI:10.1016/S0040-4020(01)96061-2