52833-93-9 Usage
Uses
Used in Pharmaceutical Industry:
2-Amino-5-chloropyridine-3-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the molecular structures of potential drugs. Its presence in drug molecules can contribute to enhancing their therapeutic effects and targeting specific biological pathways.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Amino-5-chloropyridine-3-carboxylic acid is utilized as a building block in the development of new agrochemicals, such as pesticides and herbicides. Its chemical properties allow it to be a component in the creation of compounds that can effectively control, repel, or kill pests and weeds, thereby increasing crop yields and protecting agricultural produce.
Used in Organic Synthesis:
2-Amino-5-chloropyridine-3-carboxylic acid is employed as a versatile reagent in organic synthesis, where it can be used to construct a wide range of organic compounds. Its unique functional groups enable it to participate in various chemical reactions, facilitating the formation of complex organic molecules for use in research and industry.
Used in Drug Discovery:
2-Amino-5-chloropyridine-3-carboxylic acid is also used as a starting material in drug discovery processes, where its chemical properties are exploited to design and develop new drugs with improved efficacy and selectivity. The exploration of its antimicrobial and anticancer properties makes it a promising candidate for the creation of novel therapeutic agents to combat resistant infections and cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 52833-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,3 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52833-93:
(7*5)+(6*2)+(5*8)+(4*3)+(3*3)+(2*9)+(1*3)=129
129 % 10 = 9
So 52833-93-9 is a valid CAS Registry Number.
52833-93-9Relevant academic research and scientific papers
Regioselective palladium-catalyzed Suzuki–Miyaura coupling reaction of 2,4,6-trihalogenopyrido[2,3-d]pyrimidines
Riadi, Yassine,Lazar, Sa?d,Guillaumet, Gérald
, p. 294 - 298 (2019/02/25)
An effective, regioselective, and novel strategy to the access of 2,4,6-trisubstituted pyrido[2,3-d]pyrimidines is developed from the corresponding 2,4,6-trihalogenopyrido[2,3-d]pyrimidine through a Suzuki–Miyaura coupling reaction involving a novel regioselective halogen discrimination.
Inhibiting the growth of weeds with 2-substituted pyrdidopyimidines and salts thereof
-
, (2008/06/13)
2-Substituted pyridopyrimidines and their alkali and alkylamine salts as herbicides, and processes for the synthesis of starting materials leading to the preparation thereof.
