Benzenecarboximidic acid, 4-methyl-3-nitro-, methyl ester

Base Information

Chemical Name:Benzenecarboximidic acid, 4-methyl-3-nitro-, methyl ester
CAS No.:166522-39-0
Molecular Formula:C9H10N2O3
Molecular Weight:194.19
Hs Code.:
DSSTox Substance ID:DTXSID60434125
Wikidata:Q82248452

Synonyms:166522-39-0;Benzenecarboximidic acid, 4-methyl-3-nitro-, methyl ester;DTXSID60434125

Suppliers and Price of Benzenecarboximidic acid, 4-methyl-3-nitro-, methyl ester

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 1 raw suppliers

Chemical Property of Benzenecarboximidic acid, 4-methyl-3-nitro-, methyl ester

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:194.06914219
Heavy Atom Count:14
Complexity:237

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C=C(C=C1)C(=N)OC)[N+](=O)[O-]

Technology Process of Benzenecarboximidic acid, 4-methyl-3-nitro-, methyl ester

There total 2 articles about Benzenecarboximidic acid, 4-methyl-3-nitro-, methyl ester 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:

: 67-56-1
methanol

: 939-79-7
4-cyano-2-nitrotoluene

: 166522-39-0
4-methyl-3-nitro-benzimidic acid methyl ester

Guidance literature:: With hydrogenchloride; chloroform;

Reference yield:

: 104-85-8
para-methylbenzonitrile

: 166522-39-0
4-methyl-3-nitro-benzimidic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: concentrated sulfuric acid; HNO₃

2: chloroform; HCl

With hydrogenchloride; chloroform; sulfuric acid; nitric acid;