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Quinoline, 1,2,3,4-tetrahydro-2-(1-methylethyl)-, (2S)- (9CI)

Base Information
  • Chemical Name:Quinoline, 1,2,3,4-tetrahydro-2-(1-methylethyl)-, (2S)- (9CI)
  • CAS No.:608525-30-0
  • Molecular Formula:C12H17N
  • Molecular Weight:175.27008
  • Hs Code.:
  • Mol file:608525-30-0.mol
Quinoline, 1,2,3,4-tetrahydro-2-(1-methylethyl)-, (2S)- (9CI)

Synonyms:Quinoline, 1,2,3,4-tetrahydro-2-(1-methylethyl)-, (2S)- (9CI)

Suppliers and Price of Quinoline, 1,2,3,4-tetrahydro-2-(1-methylethyl)-, (2S)- (9CI)
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Quinoline, 1,2,3,4-tetrahydro-2-(1-methylethyl)-, (2S)- (9CI)
Chemical Property:
  • PSA:12.03000 
  • LogP:3.20730 
Purity/Quality:
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Technology Process of Quinoline, 1,2,3,4-tetrahydro-2-(1-methylethyl)-, (2S)- (9CI)

There total 21 articles about Quinoline, 1,2,3,4-tetrahydro-2-(1-methylethyl)-, (2S)- (9CI) 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 (R)-(-)-5,5’-bis(diphenyl;phosphine)-2,2,2’,2’-tetrafluoro-4,4’-bi-1,3-benzodioxole; bis(1,5-cyclooctadiene)diiridium(I) dichloride; hydrogen; iodine; In tetrahydrofuran; at 20 ℃; for 24h; under 36201.3 Torr; optical yield given as %ee; enantioselective reaction; Autoclave;
DOI:10.1039/c002668a
Guidance literature:
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; ZhaoPhos; hydrogen; In dichloromethane; isopropyl alcohol; at 25 ℃; for 48h; under 30402 Torr; enantioselective reaction;
DOI:10.1039/c5sc04712a
Guidance literature:
With diphenyl hydrogen phosphate; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; In benzene; at 60 ℃; for 12h;
DOI:10.1055/s-2006-939706
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