3-Methyl-2-nitro-1-benzothiophene

Base Information

Chemical Name:3-Methyl-2-nitro-1-benzothiophene
CAS No.:33357-85-6
Molecular Formula:C₉H₇NO₂S
Molecular Weight:193.226
Hs Code.:
NSC Number:108796
DSSTox Substance ID:DTXSID40296324
Wikidata:Q82036868

Synonyms:3-methyl-2-nitro-1-benzothiophene;33357-85-6;NSC108796;DTXSID40296324;AKOS025395157;NSC-108796

Suppliers and Price of 3-Methyl-2-nitro-1-benzothiophene

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 3-Methyl-2-nitro-1-benzothiophene

Chemical Property:

Vapor Pressure:0.000307mmHg at 25°C
Boiling Point:331.1°C at 760 mmHg
Flash Point:154°C
Density:1.368g/cm³
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:193.01974964
Heavy Atom Count:13
Complexity:216

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(SC2=CC=CC=C12)[N+](=O)[O-]

Technology Process of 3-Methyl-2-nitro-1-benzothiophene

There total 4 articles about 3-Methyl-2-nitro-1-benzothiophene 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:

: 1455-18-1
3-methylbenzothiophene

: 33357-85-6
3-methyl-2-nitrobenzo[b]thiophene

Guidance literature:: With nitric acid; acetic acid;
DOI:10.1021/ja01109a512

Reference yield:

: 875257-99-1
(2-acetyl-phenylsulfanyl)-acetic acid

: 33357-85-6
3-methyl-2-nitrobenzo[b]thiophene

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid anhydride

2: acetic acid; nitric acid

With nitric acid; acetic anhydride; acetic acid;

Reference yield:

: 3133-78-6
3-methylbenzo[b]thiophene-2-carboxylic acid

: 33357-85-6
3-methyl-2-nitrobenzo[b]thiophene

Guidance literature:: Multi-step reaction with 2 steps

1: copper oxide-chromium oxide; quinoline / 170 °C

2: acetic acid; nitric acid

With quinoline; copper oxide-chromium oxide; nitric acid; acetic acid;