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5-(4-FORMYLPHENYL)NICOTINIC ACID is a derivative of Nicotinic Acid (N429250), which is a precursor of the essential coenzymes NAD (Nicotinamide adenine dinucleotide) and NADP (Nicotinamide adenine dinucleotide phosphate). It is widely distributed in nature and can be found in various sources such as liver, fish, yeast, and cereal grains. The term "niacin" is also used to refer to nicotinamide or other derivatives that exhibit the biological activity of nicotinic acid. 5-(4-FORMYLPHENYL)NICOTINIC ACID serves as a vital vitamin and enzyme cofactor in various biological processes.

566198-28-5

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566198-28-5 Usage

Uses

Used in Pharmaceutical Industry:
5-(4-FORMYLPHENYL)NICOTINIC ACID is used as a pharmaceutical compound for its potential role in the treatment and prevention of pellagra, a disease caused by dietary deficiency of niacin. As a derivative of nicotinic acid, it contributes to the synthesis of NAD and NADP, which are crucial for cellular metabolism and energy production.
Used in Nutritional Supplements:
In the nutritional supplement industry, 5-(4-FORMYLPHENYL)NICOTINIC ACID is used as an ingredient to support overall health and well-being. It helps maintain adequate levels of niacin in the body, which is essential for converting food into energy and supporting the proper functioning of the nervous system.
Used in Research and Development:
5-(4-FORMYLPHENYL)NICOTINIC ACID is utilized as a research compound for studying the structure, function, and potential applications of niacin and its derivatives. This can lead to the development of new drugs, therapies, and supplements that target various health conditions and promote overall health.
Used in Enzyme Cofactor Production:
In the biotechnology industry, 5-(4-FORMYLPHENYL)NICOTINIC ACID is used as a key component in the production of enzyme cofactors, such as NAD and NADP. These cofactors play a vital role in numerous enzymatic reactions, including redox reactions, and are essential for maintaining cellular health and function.
Used in Agricultural Applications:
5-(4-FORMYLPHENYL)NICOTINIC ACID can be employed in the agricultural sector as a component in the development of fortified animal feed or fertilizers. By providing a source of niacin, it can help improve the health and productivity of livestock and promote the growth of crops.

Check Digit Verification of cas no

The CAS Registry Mumber 566198-28-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,6,1,9 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 566198-28:
(8*5)+(7*6)+(6*6)+(5*1)+(4*9)+(3*8)+(2*2)+(1*8)=195
195 % 10 = 5
So 566198-28-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO3/c15-8-9-1-3-10(4-2-9)11-5-12(13(16)17)7-14-6-11/h1-8H,(H,16,17)

566198-28-5SDS

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 5-(4-formylphenyl)pyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:566198-28-5 SDS

566198-28-5Downstream Products

566198-28-5Relevant articles and documents

Suzuki cross-coupling reactions using reverse-phase glass beads in aqueous media

Lawson Daku, Kokovi M.,Newton, Roger F.,Pearce, Simon P.,Vile, Julia,Williams, Jonathan M. J.

, p. 5095 - 5098 (2007/10/03)

Reverse-phase glass beads have been employed in Suzuki reactions to provide, in aqueous media, a route to diverse polar substrates in good yield and with low levels of palladium leaching.

Synthesis of formylphenylpyridinecarboxylic acids using Suzuki-Miyaura coupling reactions

Meier, Peter,Legraverant, Stephanie,Mueller, Sascha,Schaub, Josette

, p. 551 - 554 (2007/10/03)

Formylphenylboronic acids were coupled with bromopyridylcarboxylic acids in the presence of a palladium catalyst. The yields of the different biaryls are strongly dependant on the substitution pattern of the two coupling partners. The electronic and steric effects of these are discussed.

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