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5-Tert-butyl-2-nitrophenol

Base Information Edit
  • Chemical Name:5-Tert-butyl-2-nitrophenol
  • CAS No.:5651-77-4
  • Molecular Formula:C10H13NO3
  • Molecular Weight:195.218
  • Hs Code.:
  • European Community (EC) Number:809-298-4
  • DSSTox Substance ID:DTXSID50474752
  • Wikidata:Q82304872
  • Mol file:5651-77-4.mol
5-Tert-butyl-2-nitrophenol

Synonyms:5-tert-butyl-2-nitrophenol;5651-77-4;Phenol, 5-(1,1-dimethylethyl)-2-nitro-;2-nitro-5-tert-butylphenol;SCHEMBL1027772;DTXSID50474752;FQVUUPPMBGPBRL-UHFFFAOYSA-N;ZB1070;AKOS006343093

Suppliers and Price of 5-Tert-butyl-2-nitrophenol
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 13 raw suppliers
Chemical Property of 5-Tert-butyl-2-nitrophenol Edit
Chemical Property:
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:195.08954328
  • Heavy Atom Count:14
  • Complexity:216
Purity/Quality:

99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)C1=CC(=C(C=C1)[N+](=O)[O-])O
Technology Process of 5-Tert-butyl-2-nitrophenol

There total 6 articles about 5-Tert-butyl-2-nitrophenol 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 nitric acid; acetic acid; In water; at 0 - 20 ℃; for 1.25h;
Guidance literature:
With sodium nitrate; sulfuric acid; sodium nitrite; In diethyl ether; Title compound not separated from byproducts;
DOI:10.1016/S0040-4039(00)87910-1
Guidance literature:
Multi-step reaction with 3 steps
1: HNO3 / acetic acid; acetic anhydride
2: (alkaline hydrolysis)
3: (i) NaNO2, aq. H2SO4, (ii) (heating), aq. H2SO4
With nitric acid; In acetic anhydride; acetic acid;
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