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4-Nitrophenyl 30-hydroxytriacontanoate

Base Information Edit
  • Chemical Name:4-Nitrophenyl 30-hydroxytriacontanoate
  • CAS No.:132910-95-3
  • Molecular Formula:C36H63NO5
  • Molecular Weight:589.9
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80564453
  • Wikidata:Q82449143
  • Mol file:132910-95-3.mol
4-Nitrophenyl 30-hydroxytriacontanoate

Synonyms:132910-95-3;4-NITROPHENYL 30-HYDROXYTRIACONTANOATE;DTXSID80564453

Suppliers and Price of 4-Nitrophenyl 30-hydroxytriacontanoate
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 3 raw suppliers
Chemical Property of 4-Nitrophenyl 30-hydroxytriacontanoate Edit
Chemical Property:
  • XLogP3:14.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:31
  • Exact Mass:589.47062411
  • Heavy Atom Count:42
  • Complexity:600
Purity/Quality:

98%min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC=C1[N+](=O)[O-])OC(=O)CCCCCCCCCCCCCCCCCCCCCCCCCCCCCO
Technology Process of 4-Nitrophenyl 30-hydroxytriacontanoate

There total 11 articles about 4-Nitrophenyl 30-hydroxytriacontanoate 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 boron trifluoride diethyl etherate; In chloroform; for 28h; Ambient temperature;
Guidance literature:
Multi-step reaction with 7 steps
1: 12.3 g / p-TsOH / 24 h / Heating
2: pyridinium chlorochromate, 4A molecular sieves / CH2Cl2 / 0.33 h / Ambient temperature
4: 90 percent / H2 / 10percent Pd/C / ethyl acetate / 24 h / Ambient temperature
5: 86 percent / 85.5percent KOH / aq. ethanol / 2.5 h / 60 °C
6: 95 percent / pyridine / 1.5 h / Ambient temperature
7: 88 percent / BF3*Et2O / CHCl3 / 28 h / Ambient temperature
With pyridine; potassium hydroxide; 4 A molecular sieve; boron trifluoride diethyl etherate; hydrogen; toluene-4-sulfonic acid; pyridinium chlorochromate; palladium on activated charcoal; In ethanol; dichloromethane; chloroform; ethyl acetate;
Guidance literature:
Multi-step reaction with 6 steps
1: pyridinium chlorochromate, 4A molecular sieves / CH2Cl2 / 0.33 h / Ambient temperature
3: 90 percent / H2 / 10percent Pd/C / ethyl acetate / 24 h / Ambient temperature
4: 86 percent / 85.5percent KOH / aq. ethanol / 2.5 h / 60 °C
5: 95 percent / pyridine / 1.5 h / Ambient temperature
6: 88 percent / BF3*Et2O / CHCl3 / 28 h / Ambient temperature
With pyridine; potassium hydroxide; 4 A molecular sieve; boron trifluoride diethyl etherate; hydrogen; pyridinium chlorochromate; palladium on activated charcoal; In ethanol; dichloromethane; chloroform; ethyl acetate;
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