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135270-13-2

Base Information Edit
  • Chemical Name:135270-13-2
  • CAS No.:135270-13-2
  • Molecular Formula:C12H11F2N3O
  • Molecular Weight:251.236
  • Hs Code.:
  • Mol file:135270-13-2.mol
135270-13-2

Synonyms:1-(((2R,3R)-2-(2,4-difluorophenyl)-3-methyloxiran-2-yl)methyl)-1H-1,2,4-triazole;Efinaconazole Related Impurity 6;1-[[(2R,3R)-2-(2,4-Difluorophenyl)-3-methyl-2-oxiranyl]methyl]-1H-1,2,4-triazole

Suppliers and Price of 135270-13-2
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
  • TRC
  • (2R,3R)-2-(2,4-Difluorophenyl)-3-methyl-2-[(1H-1,2,4-triazol-1-yl)methyl]oxirane
  • 1mg
  • $ 185.00
Total 5 raw suppliers
Chemical Property of 135270-13-2 Edit
Chemical Property:
  • Boiling Point:371.6±52.0 °C(Predicted) 
  • PKA:2.75±0.10(Predicted) 
  • PSA:43.24000 
  • Density:1.41±0.1 g/cm3(Predicted) 
  • LogP:1.87050 
Purity/Quality:

99% *data from raw suppliers

(2R,3R)-2-(2,4-Difluorophenyl)-3-methyl-2-[(1H-1,2,4-triazol-1-yl)methyl]oxirane *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses (2R,3R)-2-(2,4-Difluorophenyl)-3-methyl-2-[(1H-1,2,4-triazol-1-yl)methyl]oxirane is a useful synthetic intermediate in the synthesis of (2R,3S)-Efinaconazole (E435080); the 2R,3S-enantiomer of Efinaconazole (E435070) which is a topical antifungal for onychomycosis.
Technology Process of 135270-13-2

There total 91 articles about 135270-13-2 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:
(2R,3R)-2-(2,4-Difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-2,3-butanediol; With methanesulfonyl chloride; triethylamine; In tetrahydrofuran; at 0 ℃; for 0.333333h;
With tetrabutylammomium bromide; sodium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 12h; enantioselective reaction;
DOI:10.1021/acs.orglett.1c02588
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