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3-Pyrrolidin-3-ylpyridine, commonly known as nicotine, is a highly addictive chemical compound predominantly found in tobacco products. It functions as a stimulant to the central nervous system, enhancing dopamine levels in the brain, which in turn generates sensations of pleasure and reward. This addictive nature has made nicotine a major contributor to preventable death and disease globally.

150281-46-2

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150281-46-2 Usage

Uses

Used in Tobacco Products:
Nicotine is used as an addictive substance in tobacco products for its ability to stimulate the central nervous system and induce feelings of pleasure and reward. Its presence in these products is a significant public health concern due to its highly addictive properties.
Used in Research and Pharmaceutical Development:
Nicotine is also used in scientific research and pharmaceutical development as a model compound to study addiction and to develop treatments for nicotine dependence and smoking cessation. Understanding its effects on the brain can aid in the creation of therapies to help individuals quit smoking and reduce tobacco-related health risks.
Used in Nicotine Replacement Therapies:
In some cases, nicotine is used as a component in nicotine replacement therapies (NRTs), which are designed to help smokers gradually reduce their dependence on tobacco by providing a controlled dose of nicotine without the harmful chemicals found in tobacco smoke. This application aims to assist individuals in quitting smoking by managing withdrawal symptoms and cravings.

Check Digit Verification of cas no

The CAS Registry Mumber 150281-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,2,8 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 150281-46:
(8*1)+(7*5)+(6*0)+(5*2)+(4*8)+(3*1)+(2*4)+(1*6)=102
102 % 10 = 2
So 150281-46-2 is a valid CAS Registry Number.

150281-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Pyrrolidin-3-yl)pyridine hydrochloride

1.2 Other means of identification

Product number -
Other names 3-Pyrrolidinopyridine oxalate

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:150281-46-2 SDS

150281-46-2Relevant academic research and scientific papers

BENZIMIDAZOLE AND AZA-BENZIMIDAZOLE CARBOXAMIDES

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Page/Page column 39, (2010/05/14)

This invention provides compounds of Formula I which are PAFR antagonists: I and the pharmaceutically acceptable salts thereof. The compounds are useful for treating PAF-mediated disorders, and can be used in methods for treating atherosclerosis and preve

BIARYL CARBOXAMIDES

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Page/Page column 37-38, (2010/08/04)

This invention provides compounds of Formula (I) which are PAFR antagonists: Formula (I) and the pharmaceutically acceptable salts thereof. The compounds are useful for treating PAF-mediated disorders, and can be used in methods for treating atherosclerosis and preventing or reducing risk for atherosclerotic disease events. The compounds are also useful for treating or ameliorating pain, e.g. inflammatory pain and/or nociceptive pain, and for treating or ameliorating autoimmune and/or inflammatory diseases, among other conditions.

7-substituted quinolones and naphthyridones as antibacterial agents

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, (2008/06/13)

7-Substituted quinolones and naphthyridones are described as antibacterial agents as well as a process for their manufacture, compositions therefor, wherein the 7-substituent is a pyrrolidine ring substituted at the 3-position by a substituted aromatic hydrocarbon or a heteroaromatic group.

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