101066-61-9 Usage
Description
2-Chloroisonicotinaldehyde is a white to yellow solid that serves as a versatile reagent in various chemical synthesis processes. It is characterized by its unique chemical structure, which includes a chloro group attached to a pyridine ring and an aldehyde functional group, making it a valuable intermediate in the synthesis of complex organic molecules.
Uses
Used in Chemoenzymic Synthesis:
2-Chloroisonicotinaldehyde is used as a reagent in the chemoenzymic synthesis of α-fluoro β-hydroxy carboxylic esters. Its presence in this process allows for the efficient and selective formation of these esters, which are important building blocks in the development of pharmaceuticals and agrochemicals.
Used in Combinatorial Synthesis:
In the field of combinatorial chemistry, 2-Chloroisonicotinaldehyde is utilized as a reagent for the synthesis of methylene sulfonamides and related compounds. These compounds are of interest as potential kinase inhibitors, which can be used in the development of targeted therapies for various diseases, including cancer and inflammatory disorders.
Used in Pharmaceutical Industry:
2-Chloroisonicotinaldehyde is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it an essential component in the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Chloroisonicotinaldehyde is employed as a building block for the synthesis of novel agrochemicals. Its incorporation into these compounds can lead to the development of more effective and environmentally friendly pesticides and herbicides.
Overall, 2-Chloroisonicotinaldehyde is a valuable reagent with a wide range of applications across different industries, particularly in the development of pharmaceuticals and agrochemicals. Its unique chemical properties and versatility in synthesis processes make it an essential component in the creation of innovative and effective products.
Check Digit Verification of cas no
The CAS Registry Mumber 101066-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,6 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 101066-61:
(8*1)+(7*0)+(6*1)+(5*0)+(4*6)+(3*6)+(2*6)+(1*1)=69
69 % 10 = 9
So 101066-61-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClNO/c7-6-3-5(4-9)1-2-8-6/h1-4H
101066-61-9Relevant articles and documents
METHODS FOR TREATING CHRONIC PAIN USING 3-ARYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES, 3-HETEROARYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS
-
, (2010/11/29)
Disclosed herein are methods of treating a patient suffering from one or more types of chronic pain using compounds of Formulas 1 and 2 wherein the variables have the meaning disclosed in the specification
Practical routes toward the synthesis of 2-halo- and 2-alkylamino-4-pyridinecarboxaldehydes
Frey, Lisa F,Marcantonio, Karen,Frantz, Doug E,Murry, Jerry A,Tillyer, Richard D,Grabowski, Edward J.J,Reider, Paul J
, p. 6815 - 6818 (2007/10/03)
We recently required an efficient synthesis of 2-halo- and 2-alkylamino-4-pyridinecarboxaldehydes. Several routes to these compounds were investigated resulting in efficient and practical procedures from readily available and inexpensive starting materials.
Substituted imidazole compounds
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, (2008/06/13)
This invention relates to a novel group of imidazole compounds, processes for the preparation thereof, the use thereof in treating cytokine mediated diseases and pharmaceutical compositions for use in such therapy.
