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6972-40-3

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6972-40-3 Usage

Type of compound

Synthetic chemical

Use in research

Study the effects of neurotoxicity and develop treatments for Parkinson's disease

Conversion in the body

Converted to a toxic metabolite called MPP+

Effect on the brain

Causes damage to dopaminergic neurons, leading to Parkinson's-like symptoms

Notoriety

Gained attention in the 1980s when drug users developed Parkinson's-like symptoms after taking synthetic heroin contaminated with MPTP

Value in research

Has been useful in advancing our understanding of the mechanisms of Parkinson's disease and developing new treatments for the condition

Animal models

Has been used in animal models of Parkinson's disease to study potential treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 6972-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6972-40:
(6*6)+(5*9)+(4*7)+(3*2)+(2*4)+(1*0)=123
123 % 10 = 3
So 6972-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N/c1-2-8-6-4-3-5-7-8/h3-4H,2,5-7H2,1H3

6972-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-3,6-dihydro-2H-pyridine

1.2 Other means of identification

Product number -
Other names 1-Aethyl-1,2,3,6-tetrahydro-pyridin

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:6972-40-3 SDS

6972-40-3Downstream Products

6972-40-3Relevant articles and documents

trans-Dihydroxypiperidines: Synthesis, Stereochemistry, and Anti-HIV Activity

Grishina,Borisenko,Nosan',Veselov,Ashkinadze,Karamov,Kornilaeva,Zefirov

, p. 195 - 199 (2007/10/03)

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