88912-25-8 Usage
Uses
Used in Pharmaceutical Industry:
4,6-Dichloro-2-pyridinecarboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its antimicrobial, antifungal, and herbicidal properties. It serves as a valuable building block in the development of drugs targeting a range of diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 4,6-Dichloro-2-pyridinecarboxylic acid is utilized as a precursor in the production of crop protection products. Its herbicidal and antifungal activities contribute to the development of effective solutions for managing pests and diseases in agriculture.
Used in Cancer Research and Treatment:
4,6-Dichloro-2-pyridinecarboxylic acid is studied for its potential use in the treatment of cancer due to its ability to inhibit specific enzymes and biological pathways. It is being explored as a possible therapeutic agent for various types of cancer, offering new avenues for cancer treatment and management.
Used in Chemistry:
4,6-Dichloro-2-pyridinecarboxylic acid also holds significance in the field of chemistry, where it is employed in various chemical reactions and processes. Its unique structure and functional groups make it a useful component in the synthesis of other organic compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 88912-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,1 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88912-25:
(7*8)+(6*8)+(5*9)+(4*1)+(3*2)+(2*2)+(1*5)=168
168 % 10 = 8
So 88912-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl2NO2/c7-3-1-4(6(10)11)9-5(8)2-3/h1-2H,(H,10,11)
88912-25-8Relevant academic research and scientific papers
HETEROARYL COMPOUNDS AND THEIR USE
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Page/Page column 98-99, (2018/07/29)
The application is directed to compounds of formula (I): and their salts and solvates, wherein R1, R2, R3, A1, A2, A3, and n are as set forth in the specification, as well as to a method for their preparation, pharmaceutical compositions comprising the same, and use thereof for the treatment and/or prevention of a lysosomal storage disease, such as Gaucher's, and other diseases or disorders that are synucleinopathies.
N-(phenylsulfonyl)picolinamide derivatives, process for producing the same, and herbicide
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, (2008/06/13)
A herbicide containing as the active ingredient an N-(henylsulfonyl)picolinamide derivative represented by general formula (I) wherein X reprcsents a halogeno, a C1-4 alkyl, a C1-4 haloalkyl, a C1-4 alkoxy, a C1-4 haloalkoxy, a (C1-4 alkoxy)carbonyl, a [di(C1-4 alkyl)amino]sulfonyl, an [N—(C1-4 alkyl)-N—(C1-4 alkoxy)amino]sulfonyl, a (C1-4 alkylamino)sulfonyl, a C1-4 alkylthio, a C1-4 alkylsulfinyl, a C1-4 alkylsulfonyl, or nitro; n is an integer of 0 to 5; Y represets a halogeno, a C1-4 alkyl, a C1-4 haloalkyl, a C1-4 alkoxy, C1-4 haloalkoxy, a C1-4 alkylthio, a C1-4 haloalkylthio, amino, a C1-4 alkylamino, a di(C1-4 alkyl)amino, a (C1-4 alkoxy) C1-4 alkyl, a (C1-4 alkylthio) C1-4 alkyl, or nitro; and m is an integer of 0 to 4. This active ingredient is synthesized by condensing a substituted picolinic acid with a substituted benzenesulfonamide under dehydration, or by reacting the phenyl ester of a substituted picolinic acid with a substituted benzenesulfonamide in the presence of a basic compound.
