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(4-methoxypyridin-2-yl)(phenyl)methanol is a complex organic compound characterized by a unique molecular structure. It features a central methanol group, which is bonded to both a 4-methoxypyridin-2-yl moiety and a phenyl group. The 4-methoxypyridin-2-yl group consists of a pyridine ring with a methoxy substituent at the 4-position and a hydroxyl group attached to the 2-position. The phenyl group, on the other hand, is a benzene ring with a hydroxyl substituent. (4-methoxypyridin-2-yl)(phenyl)methanol is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, given its ability to act as a building block or intermediate in various chemical reactions. Its specific properties, such as solubility and reactivity, can be influenced by the presence of the methoxy and hydroxyl groups, making it a versatile molecule in organic chemistry.

29082-99-3

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29082-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29082-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,8 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29082-99:
(7*2)+(6*9)+(5*0)+(4*8)+(3*2)+(2*9)+(1*9)=133
133 % 10 = 3
So 29082-99-3 is a valid CAS Registry Number.

29082-99-3Relevant academic research and scientific papers

Intramolecular hydride addition to pyridinium salts: New routes to enantiopure dihydropyridones

Donohoe, Timothy J.,Connolly, Matthew J.,Rathi, Akshat H.,Walton, Lesley

, p. 2074 - 2077 (2011/06/22)

The transformation of a simple disubstituted pyridine into a pyridinium ion bearing an exocyclic hydroxyl group, protected as a silane, enabled an intramolecular hydride transfer reaction to take place when fluoride was used as a nucleophile. The addition

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