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Encyclopedia

Tipifarnib (S enantioMer)

Base Information Edit
  • Chemical Name:Tipifarnib (S enantioMer)
  • CAS No.:192185-71-0
  • Molecular Formula:C27H22Cl2N4O
  • Molecular Weight:489.404
  • Hs Code.:
  • Mol file:192185-71-0.mol
Tipifarnib (S enantioMer)

Synonyms:tiparfinib

Suppliers and Price of Tipifarnib (S enantioMer)
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
  • DC Chemicals
  • TipifarnibSenantiomer >98%
  • 1g
  • $ 2600.00
  • DC Chemicals
  • TipifarnibSenantiomer >98%
  • 250 mg
  • $ 1300.00
  • DC Chemicals
  • TipifarnibSenantiomer >98%
  • 100 mg
  • $ 700.00
  • Crysdot
  • TipifarnibSenantiomer 98+%
  • 100mg
  • $ 665.00
  • Crysdot
  • TipifarnibSenantiomer 98+%
  • 50mg
  • $ 490.00
  • Crysdot
  • TipifarnibSenantiomer 98+%
  • 10mg
  • $ 233.00
  • Crysdot
  • TipifarnibSenantiomer 98+%
  • 5mg
  • $ 137.00
  • ChemScene
  • TipifarnibSenantiomer 99.82%
  • 10mg
  • $ 348.00
  • ChemScene
  • TipifarnibSenantiomer 99.82%
  • 5mg
  • $ 214.00
  • ChemScene
  • TipifarnibSenantiomer 99.82%
  • 50mg
  • $ 936.00
Total 14 raw suppliers
Chemical Property of Tipifarnib (S enantioMer) Edit
Chemical Property:
  • Boiling Point:681.7±55.0 °C(Predicted) 
  • PKA:7.20±0.10(Predicted) 
  • Density:1.33±0.1 g/cm3(Predicted) 
Purity/Quality:

99% *data from raw suppliers

TipifarnibSenantiomer >98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Tipifarnib (S enantioMer)

There total 3 articles about Tipifarnib (S enantioMer) 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 sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; In tetrahydrofuran; water; at 20 ℃; for 2h;
Guidance literature:
N-[(4-chlorophenyl)((4-(3-chlorophenyl)-1-methyl-1H-quinoline-2-one)-6-yl)(1-methyl-1H-imidazole-5-yl)methyl]-2-methyl-2-propanesulfinamide [S(R)]; With hydrogenchloride; methanol; water; isopropyl alcohol; at 20 ℃; for 0.5h;
With potassium carbonate; In methanol; water; isopropyl alcohol; at 0 ℃;
Guidance literature:
6-[((S)-1-(4-methoxyphenyl)ethylamino)(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)]methyl-4-(3-chlorophenyl)-1-methyl-1H-quinolin-2-one; With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 0.583333h;
With potassium carbonate; In dichloromethane; water; at 0 ℃;
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