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1,4 DI METHYL 2,5- DI NITRO BENZENE

Base Information Edit
  • Chemical Name:1,4 DI METHYL 2,5- DI NITRO BENZENE
  • CAS No.:712-32-3
  • Molecular Formula:C8H8N2O4
  • Molecular Weight:196.163
  • Hs Code.:2904209090
  • Mol file:712-32-3.mol
1,4 DI METHYL 2,5- DI NITRO BENZENE

Synonyms:2,5-dimethyl-p-dinitrobenzene;2,5-Dinitro-1,4-dimethyl-benzol;Benzene,1,4-dimethyl-2,5-dinitro;2,5-dinitro-p-xylene;2,5-Dinitro-p-xylol;Benzene, 1,4-dimethyl-2,5-dinitro-;1,4-Dimethyl-2,5-dinitrobenzol;1,4-dimethyl-2,5-dinitro-benzene;

Suppliers and Price of 1,4 DI METHYL 2,5- DI NITRO BENZENE
Supply Marketing:Edit
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 2 raw suppliers
Chemical Property of 1,4 DI METHYL 2,5- DI NITRO BENZENE Edit
Chemical Property:
  • Melting Point:142 °C 
  • Boiling Point:326.4±37.0 °C(Predicted) 
  • PSA:91.64000 
  • Density:1.346±0.06 g/cm3(Predicted) 
  • LogP:3.16620 
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 1,4 DI METHYL 2,5- DI NITRO BENZENE

There total 11 articles about 1,4 DI METHYL 2,5- DI NITRO BENZENE 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:
Guidance literature:
With dihydrogen peroxide; In trifluoroacetic acid; for 10h; Ambient temperature;
Guidance literature:
With Iron(III) nitrate nonahydrate; phosphorus pentoxide; In neat (no solvent); at 20 ℃; for 6h; Milling; Green chemistry;
DOI:10.1016/j.tetlet.2021.153087
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