473837-10-4 Usage
Description
3,4-Dichloro-5-pyridinecarboxylic acid is a chemical compound with the molecular formula C6H3Cl2NO2. It is a derivative of pyridine and is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. This white crystalline solid is slightly soluble in water and stable under normal conditions. It is known to possess antibacterial and antifungal properties, making it a versatile intermediate in drug manufacturing and a valuable research reagent in organic synthesis and chemical biology.
Uses
Used in Pharmaceutical Industry:
3,4-Dichloro-5-pyridinecarboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of drugs with potent antibacterial and antifungal properties. Its unique structure allows for the creation of compounds that can effectively target and combat a range of microbial infections.
Used in Agrochemical Industry:
In the agrochemical sector, 3,4-Dichloro-5-pyridinecarboxylic acid is utilized as a building block for the development of pesticides and fungicides. Its inherent antimicrobial characteristics make it a suitable candidate for protecting crops from diseases and pests, thereby ensuring higher yields and crop quality.
Used in Organic Synthesis Research:
3,4-Dichloro-5-pyridinecarboxylic acid serves as a valuable research reagent in the field of organic synthesis. It is employed in the development and optimization of synthetic pathways, enabling the creation of novel organic compounds with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.
Used in Chemical Biology Research:
As a research reagent in chemical biology, 3,4-Dichloro-5-pyridinecarboxylic acid aids scientists in understanding the interactions between small molecules and biological systems. Its use in this field contributes to the advancement of knowledge on molecular mechanisms and the development of targeted therapies and diagnostic tools.
Check Digit Verification of cas no
The CAS Registry Mumber 473837-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,8,3 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 473837-10:
(8*4)+(7*7)+(6*3)+(5*8)+(4*3)+(3*7)+(2*1)+(1*0)=174
174 % 10 = 4
So 473837-10-4 is a valid CAS Registry Number.
473837-10-4Relevant articles and documents
Strategies for the selective functionalization of dichloropyridines at various sites
Marzi, Elena,Bigi, Anna,Schlosser, Manfred
, p. 1371 - 1376 (2001)
Whereas 2,3-dichloropyridine and 2,5-dichloro-4-(lithiooxy)-pyridine undergo deprotonation exclusively at the 4- and 2-positions, respectively, optional site selectivity can be implemented with 2,5- and 3,4-dichloropyridine (which are attacked, depending on the choice of the reagents, at either the 4- or 6- and either the 2- and 5-positions, respectively). Upon treatment with lithium diisopropylamide, 2,4-dichloro-3-iodopyridine, 3,5-dichloro-4-bromopyridine and 2,6-dichloro-3-iodopyridine afford 5-, 2- and 4-lithiated intermediates, but the latter isomerize instantaneously to species in which lithium and iodine have swapped places, the driving force being the low basicity of C-Li bonds when flanked by two neighboring halogens.
