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94163-98-1

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94163-98-1 Usage

Common uses

Inducing Parkinson's disease-like symptoms in animal models for scientific research

Functionality

Neurotoxin that selectively destroys dopaminergic neurons in the brain, leading to motor deficits and behavioral changes characteristic of Parkinson's disease

Check Digit Verification of cas no

The CAS Registry Mumber 94163-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,6 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94163-98:
(7*9)+(6*4)+(5*1)+(4*6)+(3*3)+(2*9)+(1*8)=151
151 % 10 = 1
So 94163-98-1 is a valid CAS Registry Number.

94163-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Pyridine, 1,2,3,6-tetrahydro-4-phenyl-1-(phenylmethyl)-, hydrochloride

1.2 Other means of identification

Product number -
Other names 1-benzyl-4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride

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:94163-98-1 SDS

94163-98-1Relevant articles and documents

Synthesis and SAR study of 4-arylpiperidines and 4-aryl-1,2,3,6- tetrahydropyridines as 5-HT2C agonists

Conway, Richard J.,Valant, Celine,Christopoulos, Arthur,Robertson, Alan D.,Capuano, Ben,Crosby, Ian T.

, p. 2560 - 2564 (2012/05/05)

A series of substituted 4-arylpiperidines and a smaller family of 4-aryl-1,2,3,6-tetrahydropyridines were synthesized and their biological activity at the 5-HT2C receptor studied to determine whether either series showed noteworthy agonist activity. Structure-activity relationships were developed from the performed receptor binding assays and functional studies, and the results of the analysis are presented herein.

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