114523-69-2 Usage
Description
1(2H)-Pyridinecarboxylic acid, 5,6-dihydro-2-methoxy-, methyl ester, also known as 2-methoxynicotinic acid methyl ester, is an organic compound with the molecular formula C8H9NO3. It is a derivative of nicotinic acid and is characterized by its colorless to pale yellow liquid appearance, slightly sweet odor, and solubility in organic solvents. 1(2H)-Pyridinecarboxylic acid, 5,6-dihydro-2-methoxy-, methyl ester serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals, with potential applications in the development of novel materials and as a reagent in organic synthesis.
Uses
Used in Pharmaceutical Synthesis:
1(2H)-Pyridinecarboxylic acid, 5,6-dihydro-2-methoxy-, methyl ester is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of drug candidates, contributing to the development of new treatments for various medical conditions.
Used in Agrochemical Production:
In the agrochemical industry, 1(2H)-Pyridinecarboxylic acid, 5,6-dihydro-2-methoxy-, methyl ester is used as an intermediate in the synthesis of herbicides and insecticides. Its incorporation into these products enhances their effectiveness in controlling pests and unwanted plant growth, supporting agricultural productivity.
Used in Novel Material Development:
1(2H)-Pyridinecarboxylic acid, 5,6-dihydro-2-methoxy-, methyl ester also has potential applications in the development of novel materials, thanks to its unique chemical properties. Researchers can leverage its characteristics to create innovative materials with specific properties for various industrial applications.
Used as a Reagent in Organic Synthesis:
1(2H)-Pyridinecarboxylic acid, 5,6-dihydro-2-methoxy-, methyl ester is utilized as a reagent in organic synthesis, facilitating various chemical reactions and contributing to the production of a diverse array of organic compounds for different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 114523-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,5,2 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114523-69:
(8*1)+(7*1)+(6*4)+(5*5)+(4*2)+(3*3)+(2*6)+(1*9)=102
102 % 10 = 2
So 114523-69-2 is a valid CAS Registry Number.
114523-69-2Relevant articles and documents
A NEW METHOD FOR REGIOSELECTIVE SYNTHESIS OF 2-SUBSTITUTED 1-(METHOXYCARBONYL)-1,2-DIHYDROPYRIDINES
Shono, Tatsuya,Matsumura, Yoshihiro,Onomura, Osamu,Yamada, Yasufu
, p. 4073 - 4074 (1987)
2-Substituted 1,2-dihydropyridines including an optically active one were regioselctively prepared from 2-substituted piperidines through three intermediates, that is, (a) 1,2,3,4-tetrahydropyridines, (b) 5-bromo-6-methoxypiperidines, and (c) 1,2,3,4-tetrahydro-6-methoxypyridines.
Stereoselective synthesis of azasugars by electrochemical oxidation
Furukubo, Shigeru,Moriyama, Noriaki,Onomura, Osamu,Matsumura, Yoshihiro
, p. 8177 - 8181 (2007/10/03)
A new method using electrochemical oxidation has been exploited for the stereoselective synthesis of 2,3,6-trihydroxylated 5S-piperidine derivatives. The electrochemical method was successively used for the conversion of N-protected piperidines to N-prote
REGIOSELECTIVE INTRODUCTION OF ALKYL GROUPS TO THE POSITION α OR γ TO NITROGEN ATOM OF PIPERIDINE SKELETONS USING ANODIC OXIDATION IN A KEY STEP
Shono, Tatsuya,Terauchi, Jun,Ohki, Yoshihisa,Matsumura, Yoshihiro
, p. 6385 - 6386 (2007/10/02)
β,γ-Unsaturated N-alkoxycarbonyl-α-methoxypiperidines, which were prepared from N-alkoxypiperidines by using anodic oxidation in a key step, were regioselectively alkylated at the α-position by using Grignard reagents in the presence of BF3*Et2O, whereas in the presence of CuBr, the alkylation took place at the γ-position.
