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3-phenyl-3-(piperidin-1-yl)propan-1-ol is a complex organic compound with the molecular formula C18H25NO. It is a derivative of propane, featuring a phenyl group (C6H5) and a piperidin-1-yl group (C5H10N) attached to the propane backbone. This molecule is characterized by its hydroxyl (-OH) group, which is responsible for its alcohol properties. It is a white crystalline solid and is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs. The compound's structure and properties make it a versatile building block in organic chemistry, with potential uses in the development of medications targeting the central nervous system.

7032-86-2

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7032-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7032-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,3 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7032-86:
(6*7)+(5*0)+(4*3)+(3*2)+(2*8)+(1*6)=82
82 % 10 = 2
So 7032-86-2 is a valid CAS Registry Number.

7032-86-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-3-piperidin-1-ylpropan-1-ol

1.2 Other means of identification

Product number -
Other names 3-Piperidino-3-phenyl-propanol-(1)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:7032-86-2 SDS

7032-86-2Downstream Products

7032-86-2Relevant academic research and scientific papers

C-H Functionalization of Amino Alcohols by Osmium Tetroxide/NMO or TPAP/NMO: Protecting Group-Free Synthesis of Indolizidines (–)-223AB and 3-epi-(–)-223AB

Chen, Wei-Lun,Wang, Lee-Ya,Li, Yu-Jang

supporting information, p. 103 - 107 (2020/01/02)

The oxidative cyclization of amino alcohols by osmium tetroxide/NMO or tetrapropylammonium perruthenate (TPAP)/NMO was found to provide an N,O-acetal moiety through the trapping of the resulting iminium ion by the alcohol. These two transformations were demonstrated in the synthesis of indolizidines (–)-223AB and 3-epi-(–)-223AB.

Aminolysis of Oxetanes: Quite Efficient Catalysis by Lanthanide(III) Trifluoromethansulfonates

Crotti, Paolo,Favero, Lucilla,Macchia, Franco,Pineschi, Mauro

, p. 7089 - 7092 (2007/10/02)

Ln(III)trifluoromethansulfonates in CH2Cl2 efficiently catalyze the aminolysis of trimethylene oxide, 2-octyl-, and 2-phenyloxetane, at r.t., to give the corresponding γ-amino alcohols in very good yields.

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