1,3-Dibromo-5-methyl-2-nitrobenzene

Base Information

Chemical Name:1,3-Dibromo-5-methyl-2-nitrobenzene
CAS No.:78831-78-4
Molecular Formula:C7H5Br2NO2
Molecular Weight:294.93
Hs Code.:
DSSTox Substance ID:DTXSID60563484
Wikidata:Q82447929

Synonyms:1,3-Dibromo-5-methyl-2-nitrobenzene;78831-78-4;3,5-Dibromo-4-nitrotoluene;DTXSID60563484

Suppliers and Price of 1,3-Dibromo-5-methyl-2-nitrobenzene

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 4 raw suppliers

Chemical Property of 1,3-Dibromo-5-methyl-2-nitrobenzene

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:294.86665
Heavy Atom Count:12
Complexity:171

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 1,3-Dibromo-5-methyl-2-nitrobenzene

There total 4 articles about 1,3-Dibromo-5-methyl-2-nitrobenzene 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: 76.0%

: 7116-17-8
2,6-dibromonitroso-4-toluene

: 78831-78-4
2,6-dibromo-4-methylnitrobenzene

Guidance literature:: With dihydrogen peroxide; nitric acid; In acetic acid; for 3h;
DOI:10.1002/ejoc.200500879

Reference yield:

: 6968-24-7
2,6-Dibromo-4-methylaniline

: 78831-78-4
2,6-dibromo-4-methylnitrobenzene

Guidance literature:: With sulfuric acid; water; copper(II) sulfate; sodium sulfite; sodium nitrite; Yield given. Multistep reaction; 1) glacial AcOH, 30 min, ice bath; 2) Et₂O, 12h;
DOI:10.1021/jo00302a028