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23239-75-0

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23239-75-0 Usage

General Description

4-(Phenylmethyl)-piperidine hydrochloride is a chemical compound commonly used in the research and development of new pharmaceuticals. It is a piperidine derivative that acts as a selective dopamine reuptake inhibitor and has potential applications in the treatment of psychiatric disorders and addictive behaviors. The hydrochloride salt form of 4-(Phenylmethyl)-piperidine is more stable and water-soluble, making it a preferred form for use in scientific studies and drug formulation. 4-(PHENYLMETHYL)-PIPERIDINE HYDROCHLORIDE has shown promise in preclinical studies for its ability to modulate dopamine levels in the brain, making it a potential candidate for the development of new medications targeting dopamine-related disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 23239-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,3 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23239-75:
(7*2)+(6*3)+(5*2)+(4*3)+(3*9)+(2*7)+(1*5)=100
100 % 10 = 0
So 23239-75-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H17N.ClH/c1-2-4-11(5-3-1)10-12-6-8-13-9-7-12;/h1-5,12-13H,6-10H2;1H

23239-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-benzylpiperidine,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-Benzyl-piperidin,Hydrochlorid

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:23239-75-0 SDS

23239-75-0Relevant articles and documents

Scalable and Straightforward Synthesis of All Isomeric (Cyclo)alkylpiperidines

Subota, Andrii I.,Lutsenko, Anton O.,Vashchenko, Bohdan V.,Volochnyuk, Dmitriy M.,Levchenko, Vitalina,Dmytriv, Yurii V.,Rusanov, Eduard B.,Gorlova, Alina O.,Ryabukhin, Sergey V.,Grygorenko, Oleksandr O.

, p. 3636 - 3648 (2019/06/13)

An efficient approach towards introducing (cyclo)alkyl substituents at C-2, C-3 or C-4 positions of the piperidine ring was described. The method relied on the straightforward two-step reaction sequence based on the formal sp3–sp3 re

Benzofuran derivatives, pharmaceutical composition containing the same, and a process for the preparation of the active ingredient

-

, (2008/06/13)

The present invention is a piperazinylalkylbenzofuran derivative of the formula wherein R1 represents a C1-4 alkyl group, R2 stands for a hydrogen atom, X means an oxygen atom, Y is a hydroxyl group, Z represents a hydrogen atom, Ar′ represents a diphenylmethyl group, a pyridyl group, a partially saturated 5-membered heterocyclic group or a phenyl group, n has a value of 0 or 1, and pharmaceutically suitable acid addition salts thereof.

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