2-(Benzylthio)-5-nitrobenzonitrile

Base Information

Chemical Name:2-(Benzylthio)-5-nitrobenzonitrile
CAS No.:175135-67-8
Molecular Formula:C₁₄H₁₀N₂O₂S
Molecular Weight:270.312
Hs Code.:2930909090
DSSTox Substance ID:DTXSID00351680
Wikidata:Q82128274
Mol file:175135-67-8.mol

Synonyms:2-(benzylthio)-5-nitrobenzonitrile;175135-67-8;2-benzylsulfanyl-5-nitrobenzonitrile;2-(benzylsulfanyl)-5-nitrobenzonitrile;Benzonitrile, 5-nitro-2-[(phenylmethyl)thio]-;2-Benzylthio-5-nitrobenzonitrile;Maybridge1_001743;SCHEMBL1818633;HMS546H05;DTXSID00351680;UVENNUQTKADSQA-UHFFFAOYSA-N;CCG-53157;STL370524;AKOS016027115;FT-0703045;SR-01000642340-1

Suppliers and Price of 2-(Benzylthio)-5-nitrobenzonitrile

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

American Custom Chemicals Corporation
2-(BENZYLTHIO)-5-NITROBENZONITRILE 95.00%
5MG
$ 498.45

Alfa Aesar
2-Benzylthio-5-nitrobenzonitrile, 97%
5g
$ 115.00

Alfa Aesar
2-Benzylthio-5-nitrobenzonitrile, 97%
1g
$ 33.50

Total 6 raw suppliers

Chemical Property of 2-(Benzylthio)-5-nitrobenzonitrile

Chemical Property:

Vapor Pressure:6.82E-08mmHg at 25°C
Boiling Point:438.6°C at 760 mmHg
Flash Point:219.1°C
PSA：94.91000
Density:1.33g/cm³
LogP:4.28198
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:270.04629874
Heavy Atom Count:19
Complexity:354

Purity/Quality:

99% ^*data from raw suppliers

2-(BENZYLTHIO)-5-NITROBENZONITRILE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 20/21/22
Safety Statements: 22-36/37

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CSC2=C(C=C(C=C2)[N+](=O)[O-])C#N

Technology Process of 2-(Benzylthio)-5-nitrobenzonitrile

There total 2 articles about 2-(Benzylthio)-5-nitrobenzonitrile 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%