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2-(pyridin-2-yl)acetyl chloride, also known as 2-Acetylpyridine, is a chemical compound with the formula C7H6ClNO. It is a yellowish liquid that is commonly used as a building block in organic synthesis. Derived from pyridine and acetyl chloride, this versatile intermediate is frequently utilized in the production of a variety of products including pharmaceuticals, dyes, and fragrances. Due to its corrosive nature, it is important to handle 2-(pyridin-2-yl)acetyl chloride with care to avoid skin, eye, and respiratory system irritation.

144659-13-2

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144659-13-2 Usage

Uses

Used in Pharmaceutical Industry:
2-(pyridin-2-yl)acetyl chloride is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(pyridin-2-yl)acetyl chloride is employed as a building block for the creation of agrochemicals, enhancing crop protection and contributing to sustainable agriculture.
Used in Dye and Fragrance Industry:
2-(pyridin-2-yl)acetyl chloride is used as a raw material in the production of dyes and fragrances, providing a wide range of colorants and scents for various applications, including textiles, cosmetics, and perfumes.
Used in Organic Synthesis:
As a versatile intermediate, 2-(pyridin-2-yl)acetyl chloride is utilized in organic synthesis for the preparation of a variety of chemical compounds, expanding the scope of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 144659-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,6,5 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144659-13:
(8*1)+(7*4)+(6*4)+(5*6)+(4*5)+(3*9)+(2*1)+(1*3)=142
142 % 10 = 2
So 144659-13-2 is a valid CAS Registry Number.

144659-13-2Relevant articles and documents

Thiophene inhibitors of PDE4: Crystal structures show a second binding mode at the catalytic domain of PDE4D2

Nankervis, Jacob L.,Feil, Susanne C.,Hancock, Nancy C.,Zheng, Zhaohua,Ng, Hooi-Ling,Morton, Craig J.,Holien, Jessica K.,Ho, Patricia W.M.,Frazzetto, Mark M.,Jennings, Ian G.,Manallack, David T.,John Martin,Thompson, Philip E.,Parker, Michael W.

supporting information; experimental part, p. 7089 - 7093 (2012/01/06)

PDE4 inhibitors have been identified as therapeutic targets for a variety of conditions, particularly inflammatory diseases. We have serendipitously identified a novel class of phosphodiesterase 4 (PDE4) inhibitor during a study to discover antagonists of the parathyroid hormone receptor. X-ray crystallographic studies of PDE4D2 complexed to four potent inhibitors reveal the atomic details of how they inhibit the enzyme and a notable contrast to another recently reported thiophene-based inhibitor.

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