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3-Pyridinemethanol, 4-[[(4-ethoxyphenyl)imino]methyl]-5-hydroxy-6-methyl- is a complex organic compound with the chemical formula C16H18N2O3. It is characterized by a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and a methanol group attached to the third carbon. The compound also features a 4-ethoxyphenyl group, which is a phenyl ring with an ethoxy substituent at the fourth position, connected to the pyridine ring through an imino group. Additionally, it has a hydroxy group at the fifth position and a methyl group at the sixth position. 3-Pyridinemethanol, 4-[[(4-ethoxyphenyl)imino]methyl]-5-hydroxy-6-methyl- is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. Its structure and properties make it a versatile building block in organic chemistry, with the ability to form various derivatives and participate in a range of chemical reactions.

4943-90-2

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4943-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4943-90-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4943-90:
(6*4)+(5*9)+(4*4)+(3*3)+(2*9)+(1*0)=112
112 % 10 = 2
So 4943-90-2 is a valid CAS Registry Number.

4943-90-2Relevant academic research and scientific papers

An Improved Oxidation Method of Pyridoxine

Iwata, Masaaki

, p. 2835 - 2836 (1981)

Manganese dioxide oxidation in the presence of primary amine was found to be an efficient oxidation system for pyridoxine.

Preparation method of pyridoxal 5-phosphate monohydrate

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Paragraph 0022-0029, (2019/08/20)

The invention provides a preparation method of pyridoxal 5-phosphate monohydrate. The preparation method comprises the following steps: 1, first oxidizing pyridoxine hydrochloride to pyridoxal hydrochloride, adding sodium sulfide, then dropwise adding p-ethoxyaniline to the solution, and carrying out a reaction to produce a pyridoxal hydrochloride Schiff base; 2, adding polyphosphoric acid to thepyridoxal hydrochloride Schiff base, performing a stirring reaction, first hydrolyzing polyphosphoric acid and then performing neutralization with an alkali solution to precipitate a large amount of an orange-red solid after the reaction is completed, and filtering and washing the solid to obtain a pyridoxal 5-phosphate Schiff base; and 3, hydrolyzing the pyridoxal 5-phosphate Schiff base with a 2mol/L of alkali solution, adding an organic solvent for extracting and performing liquid separation, adding a strong acid cation exchange resin into the aqueous phase, performing stirring for 1.0 h and then performing vacuum filtration, and performing freeze drying on the filtrate to obtain pyridoxal 5-phosphate monohydrate. The preparation method of pyridoxal 5-phosphate monohydrate is simple inoperation, mild in reaction conditions, relatively high in purity and yield of the final product, and suitable for industrial application, and has relatively good economic benefits.

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