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(1-OXIDO-3-PYRIDINYL)(PHENYL)METHANOL, with the molecular formula C12H11NO2, is a white solid chemical compound that has a molecular weight of 201.22 g/mol. It is a derivative of pyridine and phenyl groups, and is widely recognized for its role as a building block in the synthesis of pharmaceuticals and agrochemicals. Additionally, it holds potential applications in the fields of materials science and organic chemistry, making it a significant compound in the realm of organic synthesis and chemical research.
Used in Pharmaceutical Industry:
(1-OXIDO-3-PYRIDINYL)(PHENYL)METHANOL is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of novel drugs with improved therapeutic properties.
Used in Agrochemical Industry:
(1-OXIDO-3-PYRIDINYL)(PHENYL)METHANOL is used as a building block in the creation of agrochemicals, specifically for the development of new pesticides and other agricultural chemicals that can enhance crop protection and yield.
Used in Materials Science:
(1-OXIDO-3-PYRIDINYL)(PHENYL)METHANOL is used as a component in the research and development of new materials, potentially contributing to advancements in material properties and applications.
Used in Organic Chemistry Research:
(1-OXIDO-3-PYRIDINYL)(PHENYL)METHANOL is used as a valuable compound in organic chemistry research for exploring new reaction pathways, understanding molecular interactions, and developing innovative synthetic methods.

39585-76-7

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39585-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39585-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,8 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39585-76:
(7*3)+(6*9)+(5*5)+(4*8)+(3*5)+(2*7)+(1*6)=167
167 % 10 = 7
So 39585-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO2/c14-12(10-5-2-1-3-6-10)11-7-4-8-13(15)9-11/h1-9,12,14H

39585-76-7Downstream Products

39585-76-7Relevant academic research and scientific papers

Magnesiation of pyridine N-oxides via iodine or bromine-magnesium exchange: A useful tool for functionalizing pyridine N-oxides

Duan, Xin-Fang,Zi-Qian, Ma.,Zhang, Fang,Zhang, Zhan-Bin

supporting information; experimental part, p. 939 - 942 (2009/06/20)

Iodo- or 2-bromopyridine N-oxides were readily magnesiated with i-PrMgCl ? LiCl via the iodine or bromine-magnesium exchange. The bromine adjacent to pyridine N-oxide (at the 2- or 6-position) can be regioselectively magnesiated in the presence of other position substituted halogens. This method was tested in various substituted pyridine N-oxide systems, and has been successfully applied to the total synthesis of caerulomycins E and A.

ENZYMATIC SYNTHESIS OF OPTICALLY ACTIVE α-HYDROXYBENZYLPYRIDINES

Takeshita, Mitsuhiro,Yoshida, Sachiko,Sato, Takumi,Akutsu, Nami

, p. 879 - 884 (2007/10/02)

Synthesis of optically active α-hydroxybenzylpyridines by asymmetric reduction of benzoylpyridines and benzoylpyridine N-oxides with baker's yeast, and enantioselective esterification of racemic α-hydroxybenzylpyridines by use of lipase PS have been described.

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