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Phenol, 2,4-dimethoxy-3-methyl-5-nitro-

Base Information Edit
  • Chemical Name:Phenol, 2,4-dimethoxy-3-methyl-5-nitro-
  • CAS No.:136763-93-4
  • Molecular Formula:C9H11NO5
  • Molecular Weight:213.19
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60452607
  • Nikkaji Number:J955.909D
  • Wikidata:Q82273344
  • Mol file:136763-93-4.mol
Phenol, 2,4-dimethoxy-3-methyl-5-nitro-

Synonyms:Phenol, 2,4-dimethoxy-3-methyl-5-nitro-;136763-93-4;2,4-Dimethoxy-3-methyl-5-nitrophenol;SCHEMBL23247932;DTXSID60452607

Suppliers and Price of Phenol, 2,4-dimethoxy-3-methyl-5-nitro-
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 1 raw suppliers
Chemical Property of Phenol, 2,4-dimethoxy-3-methyl-5-nitro- Edit
Chemical Property:
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:2
  • Exact Mass:213.06372245
  • Heavy Atom Count:15
  • Complexity:229
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(=CC(=C1OC)O)[N+](=O)[O-])OC
Technology Process of Phenol, 2,4-dimethoxy-3-methyl-5-nitro-

There total 10 articles about Phenol, 2,4-dimethoxy-3-methyl-5-nitro- 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 hydrogenchloride; In methanol; water; at 70 ℃; for 1h;
DOI:10.1021/jo0522512
Guidance literature:
Multi-step reaction with 3 steps
1: 100 percent / CHCl3 / 2 h / Heating
2: 77 percent / HNO3; acetic acid; Ac2O / 1.67 h / 0 - 5 °C
3: 100 percent / HCl / H2O; methanol / 1 h / 70 °C
With hydrogenchloride; nitric acid; acetic anhydride; acetic acid; In methanol; chloroform; water;
DOI:10.1021/jo0522512
Guidance literature:
Multi-step reaction with 4 steps
1: 73 percent / p-toluenesulfonic acid monohydrate; hydrogen peroxide; acetic acid / H2O / 1 h / 75 °C
2: 100 percent / CHCl3 / 2 h / Heating
3: 77 percent / HNO3; acetic acid; Ac2O / 1.67 h / 0 - 5 °C
4: 100 percent / HCl / H2O; methanol / 1 h / 70 °C
With hydrogenchloride; dihydrogen peroxide; nitric acid; acetic anhydride; toluene-4-sulfonic acid; acetic acid; In methanol; chloroform; water;
DOI:10.1021/jo0522512
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