91914-07-7 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Hydroxy-6-methylpyridine is used as a key intermediate in the synthesis of pharmaceuticals for its ability to form essential components of various drug molecules, contributing to the development of new medications.
Used in Pesticide Production:
In the agricultural sector, 2-Hydroxy-6-methylpyridine is utilized as a precursor in the production of pesticides, enhancing the effectiveness of these compounds in controlling pests and diseases.
Used in Organic Compound Synthesis:
2-HYDROXY-6-METHYLPYRIDINE serves as a building block in the synthesis of other organic compounds, broadening its applications in the chemical industry and research.
Used in Metal Chelation:
2-Hydroxy-6-methylpyridine is used as a chelating agent in various industrial processes due to its ability to bind metal ions, which is crucial for applications such as water treatment and metal recovery.
Used in Research Applications:
In the scientific community, 2-hydroxy-6-methylpyridine is employed in research for its potential biological activities, including studies on its antimicrobial and antitumor properties, which could lead to advancements in medicine and healthcare.
Check Digit Verification of cas no
The CAS Registry Mumber 91914-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91914-07:
(7*9)+(6*1)+(5*9)+(4*1)+(3*4)+(2*0)+(1*7)=137
137 % 10 = 7
So 91914-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO/c1-5-3-2-4-6(8)7-5/h2-4H,1H3,(H,7,8)
91914-07-7Relevant academic research and scientific papers
Demethylation of methoxypyridines with sodium trimethylsilanethiolate
Shiao, Min-Jen,Ku, Wei-Shen,Hwu, Jih Ru
, p. 323 - 328 (2007/10/02)
Demethylation of methoxypyridines was accomplished in 55-87percent yield by use of ca. 1.5-2.5 equivalents of NaSSiMe3 in 1,3-dimethyl-2-imidazolidinone at 120-180 deg C.This method was found applicable to a methoxyquinoline and methoxypyridines containing a second substituent, such as Cl, OMe, and COOMe.
The Photolysis of 1-Benzyloxy-2-pyridone and its Methyl Derivatives. Correlation with 1H NMR-derived Ground-state Conformation
Sakurai, Tadamitsu,Murakata, Yasukuni,Inoue, Hiroyasu
, p. 499 - 503 (2007/10/02)
In addition to methyl substituent effects on the reactivities of the vibrationally unrelaxed excited singlet state of 1-benzyloxy-2-pyridone (1), deuterium isotope effects on the reaction efficiencies of (1) and its methyl derivatives are discussed on the basis of their major ground-state conformations, as analysed by 1H NMR spectroscopy.It is suggested that intramolecular hydrogen abstraction of the benzylic hydrogen by the amido carbonyl oxygen in (1) competes with N-O bond cleavage in polar solvents.Effects exerted by both a methyl group and a non-polar solvent aremanifested by the predominant N-O bond cleavage in the vibrationally 'hot' excited singlet state.
