1-cyclopentyl-3-phenyl-1-propanol

Base Information

Chemical Name:1-cyclopentyl-3-phenyl-1-propanol
CAS No.:202596-55-2
Molecular Formula:C₁₄H₂₀O
Molecular Weight:204.312
Hs Code.:

Synonyms:1-cyclopentyl-3-phenyl-1-propanol

Suppliers and Price of 1-cyclopentyl-3-phenyl-1-propanol

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of 1-cyclopentyl-3-phenyl-1-propanol

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Technology Process of 1-cyclopentyl-3-phenyl-1-propanol

There total 8 articles about 1-cyclopentyl-3-phenyl-1-propanol 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: 77.0%

: 127208-26-8,127208-28-0
cis-2-(3-butenyl)-3-(2-phenylethyl)oxirane

: 202596-55-2
1-cyclopentyl-3-phenyl-1-propanol

Guidance literature:: cis-2-(3-butenyl)-3-(2-phenylethyl)oxirane; With zirconocene hydrochloride; In dichloromethane; at 20 ℃; for 0.5h;

With boron trifluoride diethyl etherate; In dichloromethane; at 0 - 20 ℃; for 2h;
DOI:10.1016/S0040-4020(97)10340-4

Reference yield: 69.0%

: 104-53-0
3-phenyl-propionaldehyde

: 1556-18-9
cyclopentyl iodide

: 202596-55-2
1-cyclopentyl-3-phenyl-1-propanol

Guidance literature:: With indium; iodine; silver(I) iodide; In water; at 20 ℃; for 48h;
DOI:10.1021/jo8000589

Reference yield: 64.0%

: 52829-98-8
1-cyclopentylethan-1-ol

: 100-51-6,185532-71-2
benzyl alcohol

: 202596-55-2
1-cyclopentyl-3-phenyl-1-propanol

Guidance literature:: With C₂₃H₂₁MnN₂O₃P⁽¹⁺⁾*Br^(1-); potassium tert-butylate; In toluene; at 135 ℃; for 20h; chemoselective reaction; Inert atmosphere; Green chemistry;
DOI:10.1002/cssc.201801660