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(S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid

Base Information
  • Chemical Name:(S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid
  • CAS No.:1380792-92-6
  • Molecular Formula:C10H10O4
  • Molecular Weight:194.184
  • Hs Code.:
  • Mol file:1380792-92-6.mol
(S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid

Synonyms:(S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid;(S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid-7

Suppliers and Price of (S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 6 raw suppliers
Chemical Property of (S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of (S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid

There total 6 articles about (S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid 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 bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate; C34H38F6FeP2; hydrogen; sodium methylate; In methanol; at 20 ℃; for 2h; under 5250.53 Torr; Overall yield = 91 %Chromat.; enantioselective reaction; Schlenk technique; Autoclave;
DOI:10.1246/bcsj.20130324
Guidance literature:
With bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate; 1,1-bis[(2S,5S)-2,5-diethylphosphetanyl]ferrocene; hydrogen; sodium methylate; In methanol; at 20 ℃; for 2h; under 5250.53 Torr; Reagent/catalyst; enantioselective reaction; Schlenk technique; Autoclave;
DOI:10.1246/bcsj.20130324
Guidance literature:
With hydrogen; sodium methylate; dichloro [(+)-1,2-bis((2R,5R)-2,5-diisopropylphosphorano)benzene]ruthenium (II)-N,N-dimethylformamide complex; In methanol; at 20 ℃; for 12h; under 7500.75 Torr; Product distribution / selectivity;
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