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6-fluoro-(2R)-2-[(2R)-2-oxiranyl]-3,4-dihydrobenzopyran

Base Information Edit
  • Chemical Name:6-fluoro-(2R)-2-[(2R)-2-oxiranyl]-3,4-dihydrobenzopyran
  • CAS No.:197706-50-6
  • Molecular Formula:C11H11FO2
  • Molecular Weight:194.206
  • Hs Code.:
  • Mol file:197706-50-6.mol
6-fluoro-(2R)-2-[(2R)-2-oxiranyl]-3,4-dihydrobenzopyran

Synonyms:6-fluoro-(2R)-2-[(2R)-2-oxiranyl]-3,4-dihydrobenzopyran

Suppliers and Price of 6-fluoro-(2R)-2-[(2R)-2-oxiranyl]-3,4-dihydrobenzopyran
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,2’R)-6-Fluoro-2-(2’-oxiranyl)chromane
  • 25mg
  • $ 1230.00
  • TRC
  • (2R,2’R)-6-Fluoro-2-(2’-oxiranyl)chromane
  • 2.5mg
  • $ 155.00
Total 6 raw suppliers
Chemical Property of 6-fluoro-(2R)-2-[(2R)-2-oxiranyl]-3,4-dihydrobenzopyran Edit
Chemical Property:
  • Boiling Point:291.7±40.0 °C(Predicted) 
  • Density:1.299±0.06 g/cm3(Predicted) 
Purity/Quality:

99.9% *data from raw suppliers

(2R,2’R)-6-Fluoro-2-(2’-oxiranyl)chromane *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses (2R,2’R)-6-Fluoro-2-(2’-oxiranyl)chromane is an intermediate to synthesize Nebivolol (rac, HCl salt, N387900) which is a β1-Adrenergic blocker.
Technology Process of 6-fluoro-(2R)-2-[(2R)-2-oxiranyl]-3,4-dihydrobenzopyran

There total 26 articles about 6-fluoro-(2R)-2-[(2R)-2-oxiranyl]-3,4-dihydrobenzopyran 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 hydride; In tetrahydrofuran; mineral oil; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1002/ejoc.200800201
Guidance literature:
With oxygen; 4-nitro-benzoic acid; [(S,S)-N,N’-bis(3,5-di-tertbutylsalicylidene)-1,2-cyclohexanediaminato(2-)]cobalt(II); In methyl tert butyl ester; toluene; at 20 ℃; for 1h; Product distribution / selectivity; Resolution of racemate;
Refernces Edit
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