3678-63-5 Usage
Description
4-Chloro-2-picoline, with the CAS number 3678-63-5, is a light yellow liquid compound that is valuable in the field of organic synthesis. It is known for its unique chemical properties that make it a versatile building block for creating a wide range of chemical products.
Uses
Used in Organic Synthesis:
4-Chloro-2-picoline is used as a key intermediate in the synthesis of various organic compounds. Its chemical structure allows for multiple reaction pathways, making it a valuable asset in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Chloro-2-picoline is used as a building block for the development of new drugs. Its unique chemical properties enable the creation of novel molecular structures with potential therapeutic applications.
Used in Agrochemical Industry:
4-Chloro-2-picoline is also utilized in the agrochemical industry for the synthesis of new pesticides and other crop protection agents. Its versatility in organic synthesis allows for the development of innovative products to address the evolving needs of modern agriculture.
Used in Specialty Chemicals:
In the specialty chemicals sector, 4-Chloro-2-picoline is employed in the production of various chemicals with specific applications, such as dyes, additives, and coatings. Its unique properties contribute to the development of high-performance materials with tailored properties for specific industries.
Check Digit Verification of cas no
The CAS Registry Mumber 3678-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3678-63:
(6*3)+(5*6)+(4*7)+(3*8)+(2*6)+(1*3)=115
115 % 10 = 5
So 3678-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H6ClN/c1-5-4-6(7)2-3-8-5/h2-4H,1H3
3678-63-5Relevant articles and documents
Chemoselective sp 2-sp3 cross-couplings: Iron-catalyzed alkyl transfer to dihaloaromatics
Malhotra, Sushant,Seng, Pamela S.,Koenig, Stefan G.,Deese, Alan J.,Ford, Kevin A.
supporting information, p. 3698 - 3701 (2013/08/23)
The chemoselective functionalization of a range of dihaloaromatics with methyl, cyclopropyl, and higher alkyl Grignard reagents via iron-catalyzed cross-coupling is described. The site selectivity of C-X (X = halogen) activation is determined by factors such as the position of the halogen on the ring, the solvent, and the nucleophile. A one-pot protocol for the chemoselective synthesis of mixed dialkyl heterocycles is achieved solely employing iron catalysis.