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2H-Pyran-2-one, tetrahydro-4-methyl-, (4S)-

Base Information Edit
  • Chemical Name:2H-Pyran-2-one, tetrahydro-4-methyl-, (4S)-
  • CAS No.:61898-56-4
  • Molecular Formula:C6H10O2
  • Molecular Weight:114.144
  • Hs Code.:
  • Mol file:61898-56-4.mol
2H-Pyran-2-one, tetrahydro-4-methyl-, (4S)-

Synonyms:(S)-3-methyl-δ-valerolactone;(S)-3-methylvalerolactone;4(S)-methyltetrahydropyran-2-one;(-)3S-methyl valerolactone;(S)-4-Methyl-tetrahydro-pyran-2-one;(4S)-4-methyltetrahydro-2H-pyran-2-one;

Suppliers and Price of 2H-Pyran-2-one, tetrahydro-4-methyl-, (4S)-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2H-Pyran-2-one, tetrahydro-4-methyl-, (4S)- Edit
Chemical Property:
  • PSA:26.30000 
  • LogP:0.95950 
Purity/Quality:
Safty Information:
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MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 2H-Pyran-2-one, tetrahydro-4-methyl-, (4S)-

There total 48 articles about 2H-Pyran-2-one, tetrahydro-4-methyl-, (4S)- 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 horse liver alcohol dehydrogenase; oxygen; catalase; 7-(trifluoromethyl)-1,10-ethyleneisoalloxazinium chloride; In aq. phosphate buffer; at 20 ℃; for 13h; pH=8; Reagent/catalyst; enantioselective reaction; Catalytic behavior; Enzymatic reaction;
DOI:10.1021/acscatal.6b01261
Guidance literature:
(R)-3-methylpentanedioic acid monomethyl ester; With lithium hydroxide; In water; at 0 ℃; for 1h; Inert atmosphere;
With lithium borohydride; In tetrahydrofuran; for 5h; Inert atmosphere; Reflux;
DOI:10.1016/j.tet.2012.05.085
Guidance literature:
C7H11O4(1-)*Li(1+); With lithium borohydride; In tetrahydrofuran; for 5h; Inert atmosphere; Reflux;
With methanol; In tetrahydrofuran; at 20 ℃; Reflux; Inert atmosphere;
DOI:10.1002/anie.201106117
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