821791-58-6 Usage
Description
4-CHLORO-1-METHYL-6-OXO-1,6-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER is a specialized chemical compound often utilized in the field of organic chemistry. It features a pyridine ring, a six-membered nitrogen-containing ring, along with ethyl ester functionality, a chlorine atom, and a methyl group. As an ester, it has potential applications in various chemical reactions, including synthesis, where esters frequently act as intermediates in the production of other chemicals. It may also serve as a reagent to introduce the 4-chloro-1-methyl-6-oxo-1,6-dihydro-pyridine-3-carboxylate group into other molecules. The precise properties such as toxicity, reactivity, and applications of this chemical would require further scientific testing and study.
Uses
Used in Organic Chemistry:
4-CHLORO-1-METHYL-6-OXO-1,6-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER is used as a chemical intermediate for the synthesis of other compounds, given its ester functionality and the presence of a pyridine ring, chlorine atom, and methyl group.
Used in Chemical Synthesis:
4-CHLORO-1-METHYL-6-OXO-1,6-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER is used as a reagent to introduce the 4-chloro-1-methyl-6-oxo-1,6-dihydro-pyridine-3-carboxylate group into other molecules, which can be crucial for the development of new chemical entities.
Used in Pharmaceutical Research:
4-CHLORO-1-METHYL-6-OXO-1,6-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER may be used as a starting material in the development of new pharmaceutical compounds, given its unique structural features that could be exploited for medicinal chemistry purposes.
Used in Material Science:
4-CHLORO-1-METHYL-6-OXO-1,6-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER could be explored for its potential in the creation of new materials, such as polymers or other advanced materials, where its structural components might impart specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 821791-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,1,7,9 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 821791-58:
(8*8)+(7*2)+(6*1)+(5*7)+(4*9)+(3*1)+(2*5)+(1*8)=176
176 % 10 = 6
So 821791-58-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H10ClNO3/c1-3-14-9(13)6-5-11(2)8(12)4-7(6)10/h4-5H,3H2,1-2H3
821791-58-6Relevant articles and documents
HETEROCYCLIC COMPOUNDS AND USES THEREOF
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, (2021/07/31)
Provided herein are novel heterocyclic compounds, for example, compounds having Formula I, I-P, II, lI-P, or III. Also provided herein are pharmaceutical compositions comprising the compounds and methods of using the same, for example, in inhibiting aldehyde dehydrogenases and/or for treating various cancers, cancer metastasis, type 2 diabetes, pulmonary arterial hypertension (PAH) or neointimal hyperplasia (NIH).
4-Anilino-5-carboxamido-2-pyridone derivatives as noncompetitive inhibitors of mitogen-activated protein kinase kinase
Spicer, Julie A.,Rewcastle, Gordon W.,Kaufman, Michael D.,Black, Shannon L.,Plummer, Mark S.,Denny, William A.,Quin III, John,Shahripour, Aurash B.,Barrett, Stephen D.,Whitehead, Christopher E.,Milbank, Jared B. J.,Ohren, Jeffrey F.,Gowan, Richard C.,Omer, Charles,Camp, Heidi S.,Esmaeil, Nadia,Moore, Kelley,Sebolt-Leopold, Judith S.,Pryzbranowski, Sally,Merriman, Ronald L.,Ortwine, Daniel F.,Warmus, Joseph S.,Flamme, Cathlin M.,Pavlovsky, Alexander G.,Tecle, Haile
, p. 5090 - 5102 (2008/03/13)
A new series of MEK1 inhibitors, the 4-anilino-5-carboxamido-2-pyridones, were designed and synthesized using a combination of medicinal chemistry, computational chemistry, and structural elucidation. The effect of variation in the carboxamide side chain,
5-SUBSTITUTED-4-`(SUBSTITUTED PHENYL)!AMINO!-2-PYRIDONE DEVIATIVES FOR USE AS MEK INHIBITORS
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Page 91, (2010/02/10)
The present invention relates to 5-substituted-4-(substituted) phenylamino-2-pyridone derivatives of formula (I), pharmaceutical compositions and methods of use thereof as MEK inhibitors. Formula (I) wherein W is formula (II), formula (III), formula (IV),
