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3-Pyridinecarboxylic acid, 4-methoxyphenyl ester, also known as nicotine, is a naturally occurring alkaloid compound that is primarily found in the nightshade family of plants, particularly in the tobacco plant. It is an odorless, colorless, and oily liquid with a molecular formula of C12H14N2O2. This chemical is known for its stimulant effects on the human body, as it acts as a neurotransmitter in the brain, affecting the release of various chemicals such as dopamine, serotonin, and norepinephrine. Nicotine is widely recognized for its addictive properties and is the primary psychoactive component in tobacco products, contributing to their addictive nature. It is also used in various pharmaceutical applications, such as nicotine replacement therapies for smoking cessation.

3468-30-2

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3468-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3468-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3468-30:
(6*3)+(5*4)+(4*6)+(3*8)+(2*3)+(1*0)=92
92 % 10 = 2
So 3468-30-2 is a valid CAS Registry Number.

3468-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxyphenyl) pyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names Methoxy-4-phenyl-nicotinat

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:3468-30-2 SDS

3468-30-2Downstream Products

3468-30-2Relevant academic research and scientific papers

Nickel-Catalyzed Decarbonylative Coupling of Aryl Esters and Arylboronic Acids

Laberge, Nicole A.,Love, Jennifer A.

, p. 5546 - 5553 (2015)

A variety of functionalized biaryls can be accessed by coupling aryl and heteroaryl esters with boronic acids in Suzuki-Miyaura-type decarbonylative cross-coupling catalyzed by an affordable catalyst system composed of Ni(cod)2 and PCy3. The methodology is tolerant of a variety of functional groups and presents an attractive alternative to the use of palladium catalysis currently used in industry to acquire such bis(hetero)aryls, but also reveals challenges associated with nickel catalysis of esters in cross-coupling chemistry.

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