Benzenecarbothioamide, N-(2-bromophenyl)-

Base Information

Chemical Name:Benzenecarbothioamide, N-(2-bromophenyl)-
CAS No.:85433-21-2
Molecular Formula:C13H10BrNS
Molecular Weight:292.199
Hs Code.:
DSSTox Substance ID:DTXSID80465916
Nikkaji Number:J1.926.002J
Wikidata:Q82292216

Synonyms:Benzenecarbothioamide, N-(2-bromophenyl)-;85433-21-2;DTXSID80465916

Suppliers and Price of Benzenecarbothioamide, N-(2-bromophenyl)-

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
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price

Total 0 raw suppliers

Chemical Property of Benzenecarbothioamide, N-(2-bromophenyl)-

Chemical Property:

Melting Point:85-86 °C
Boiling Point:371.4±44.0 °C(Predicted)
PSA：51.16000
Density:1.518±0.06 g/cm3(Predicted)
LogP:4.45720
XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:290.97173
Heavy Atom Count:16
Complexity:238

Purity/Quality:

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=C2Br

Technology Process of Benzenecarbothioamide, N-(2-bromophenyl)-

There total 7 articles about Benzenecarbothioamide, N-(2-bromophenyl)- 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: 100.0%

: 70787-27-8
N-(2-bromophenyl)benzamide

: 85433-21-2
N-(2-bromophenyl)benzothioamide

Guidance literature:: With Lawessons reagent;
DOI:10.1016/S0040-4039(03)01469-2

Reference yield:

: 615-36-1
2-bromoaniline

: 85433-21-2
N-(2-bromophenyl)benzothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / Lawesson reagent

With Lawessons reagent;
DOI:10.1016/S0040-4039(03)01469-2

Reference yield:

: 98-88-4
benzoyl chloride

: 85433-21-2
N-(2-bromophenyl)benzothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 3 h / 20 °C

2: Lawessons reagent / toluene / 2 h / Reflux; Inert atmosphere

With Lawessons reagent; triethylamine; In dichloromethane; toluene;
DOI:10.1021/acs.orglett.8b03679