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1,2,4-Trimethylphenanthrene

Base Information
  • Chemical Name:1,2,4-Trimethylphenanthrene
  • CAS No.:23189-64-2
  • Molecular Formula:C17H16
  • Molecular Weight:220.314
  • Hs Code.:2902909090
  • DSSTox Substance ID:DTXSID20177763
  • Nikkaji Number:J1.610.667D
  • Wikidata:Q83048099
  • Mol file:23189-64-2.mol
1,2,4-Trimethylphenanthrene

Synonyms:1,2,4-TRIMETHYLPHENANTHRENE;23189-64-2;Phenanthrene,1,2,4-trimethyl-;DTXSID20177763;Phenanthrene, 1,2,4-trimethyl-

Suppliers and Price of 1,2,4-Trimethylphenanthrene
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
  • American Custom Chemicals Corporation
  • 1,2,4-TMP 95.00%
  • 5MG
  • $ 496.21
Total 3 raw suppliers
Chemical Property of 1,2,4-Trimethylphenanthrene
Chemical Property:
  • Vapor Pressure:7.25E-06mmHg at 25°C 
  • Boiling Point:387.6°C at 760 mmHg 
  • Flash Point:180.3°C 
  • PSA:0.00000 
  • Density:1.066g/cm3 
  • LogP:4.91820 
  • XLogP3:5.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:220.125200510
  • Heavy Atom Count:17
  • Complexity:269
Purity/Quality:

99% *data from raw suppliers

1,2,4-TMP 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=C2C(=C1C)C=CC3=CC=CC=C32)C
Technology Process of 1,2,4-Trimethylphenanthrene

There total 12 articles about 1,2,4-Trimethylphenanthrene 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:
Multi-step reaction with 3 steps
1: 60 percent / p-toluolsulphonic acid, acetic acid / 70 h / Heating
2: BBr3 / CH2Cl2 / 1 h / -25 °C
3: NaBH4, CF3CO2H / CH2Cl2 / 28 h / 0 °C
With sodium tetrahydroborate; boron tribromide; toluene-4-sulfonic acid; acetic acid; trifluoroacetic acid; In dichloromethane;
DOI:10.1016/S0040-4020(01)96118-6
Guidance literature:
With sodium tetrahydroborate; trifluoroacetic acid; In dichloromethane; at 0 ℃; for 28h; Yield given;
DOI:10.1016/S0040-4020(01)96118-6
Guidance literature:
Multi-step reaction with 3 steps
1: 12 mg / Pd/charcoal / 0.67 h / Heating; metal bath
2: BBr3 / CH2Cl2 / 1 h / -25 °C
3: NaBH4, CF3CO2H / CH2Cl2 / 28 h / 0 °C
With sodium tetrahydroborate; boron tribromide; trifluoroacetic acid; palladium on activated charcoal; In dichloromethane;
DOI:10.1016/S0040-4020(01)96118-6
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