N-(4-bromophenyl)pentanethioamide

Base Information

Chemical Name:N-(4-bromophenyl)pentanethioamide
CAS No.:35274-23-8
Molecular Formula:C11H14BrNS
Molecular Weight:272.2046
Hs Code.:
NSC Number:509689
DSSTox Substance ID:DTXSID90392729
Mol file:35274-23-8.mol

Synonyms:N-(4-bromophenyl)pentanethioamide;35274-23-8;NSC509689;DTXSID90392729;NSC-509689;A1-05984

Suppliers and Price of N-(4-bromophenyl)pentanethioamide

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 5 raw suppliers

Chemical Property of N-(4-bromophenyl)pentanethioamide

Chemical Property:

Vapor Pressure:0.000255mmHg at 25°C
Boiling Point:323.9°C at 760 mmHg
Flash Point:149.7°C
Density:1.388g/cm³
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:271.00303
Heavy Atom Count:14
Complexity:176

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC(=S)NC1=CC=C(C=C1)Br

Technology Process of N-(4-bromophenyl)pentanethioamide

There total 4 articles about N-(4-bromophenyl)pentanethioamide 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:

: 142810-45-5
valeric acid-(4-bromo-anilide)

: 35274-23-8
N-(4-bromophenyl)pentanethioamide

Guidance literature:: With Lawessons reagent; In toluene; Inert atmosphere; Reflux;
DOI:10.1021/acs.orglett.7b03201

Reference yield:

: 106-40-1
4-bromo-aniline

: 35274-23-8
N-(4-bromophenyl)pentanethioamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere

2: Lawessons reagent / toluene / Inert atmosphere; Reflux

With Lawessons reagent; triethylamine; In dichloromethane; toluene;
DOI:10.1021/acs.orglett.7b03201