trans-2-<2'-cyclopentyl>ethanol

Base Information

Chemical Name:trans-2-<2'-cyclopentyl>ethanol
CAS No.:121374-51-4
Molecular Formula:C₁₅H₂₁NO₃
Molecular Weight:263.337
Hs Code.:

trans-2-<2'-<N-(carbobenzyloxy)amino>cyclopentyl>ethanol

Synonyms:trans-2-<2'-cyclopentyl>ethanol

Suppliers and Price of trans-2-<2'-cyclopentyl>ethanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 0 raw suppliers

Chemical Property of trans-2-<2'-cyclopentyl>ethanol

Chemical Property:

Purity/Quality:

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Technology Process of trans-2-<2'-cyclopentyl>ethanol

There total 1 articles about trans-2-<2'-cyclopentyl>ethanol 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:

Reference yield: 69.0%

: 109842-93-5,117987-10-7
trans-2-(2'-hydroxyethyl)cyclopentylamine

: 501-53-1,94274-21-2
benzyl chloroformate

: 121374-51-4
trans-2-<2'-cyclopentyl>ethanol

Guidance literature:: With sodium hydroxide; In diethyl ether; for 16h; Ambient temperature;
DOI:10.1021/jo00275a034

Reference yield: 80.0%

: 121374-51-4
trans-2-<2'-cyclopentyl>ethanol

: 98-59-9
p-toluenesulfonyl chloride

: 121374-52-5
trans-2-<2'-cyclopentyl>ethyl tosylate

Guidance literature:: With pyridine; at 4 ℃; for 16h;
DOI:10.1021/jo00275a034

Reference yield:

: 121374-51-4
trans-2-<2'-cyclopentyl>ethanol

: 121374-50-3,121374-53-6
trans-2-<-2'-cyclopentyl>ethyl p-nitrophenyl thioether

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / pyridine / 16 h / 4 °C

2: 75 percent / sodium methoxide / methanol / 16 h / 60 °C

With pyridine; sodium methylate; In methanol;
DOI:10.1021/jo00275a034