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(2R*,4aS*,5S*,8aR*)-2-(1-propyl)-5-methyldecahydroquinoline hydrochloride

Base Information Edit
  • Chemical Name:(2R*,4aS*,5S*,8aR*)-2-(1-propyl)-5-methyldecahydroquinoline hydrochloride
  • CAS No.:55785-30-3
  • Molecular Formula:C13H25N*ClH
  • Molecular Weight:231.809
  • Hs Code.:
  • Mol file:55785-30-3.mol
(2R<sup>*</sup>,4aS<sup>*</sup>,5S<sup>*</sup>,8aR<sup>*</sup>)-2-(1-propyl)-5-methyldecahydroquinoline hydrochloride

Synonyms:

Suppliers and Price of (2R*,4aS*,5S*,8aR*)-2-(1-propyl)-5-methyldecahydroquinoline hydrochloride
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (2R*,4aS*,5S*,8aR*)-2-(1-propyl)-5-methyldecahydroquinoline hydrochloride Edit
Chemical Property:
Purity/Quality:
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Technology Process of (2R*,4aS*,5S*,8aR*)-2-(1-propyl)-5-methyldecahydroquinoline hydrochloride

There total 12 articles about (2R*,4aS*,5S*,8aR*)-2-(1-propyl)-5-methyldecahydroquinoline hydrochloride 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 hydrogen; palladium on activated charcoal; In methanol; for 20h; under 760 Torr;
DOI:10.1021/jo00041a012
Guidance literature:
Multi-step reaction with 2 steps
1: 1) THF, a) -78 deg C, 45 min, b) 0 deg C, 35 min, 2) THF, a) 0 deg C, 2 h, b) r.t., 1 h
2: 60 percent / H2 / 10percent Pd/C / methanol / 20 h / 760 Torr
With hydrogen; palladium on activated charcoal; In methanol;
DOI:10.1021/jo00041a012
Guidance literature:
Multi-step reaction with 2 steps
1: zinc; acetic acid / water / 4 h / 55 °C
2: hydrogenchloride / methanol / 0.42 h
With hydrogenchloride; acetic acid; zinc; In methanol; water;
DOI:10.1021/jo4023149
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