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2-Pyridinemethanol, α-(4-hydroxyphenyl)-, also known as 2-(4-hydroxyphenyl)pyridine-3-methanol or 4-(2-hydroxymethylpyridin-3-yl)phenol, is an organic compound with the chemical formula C11H11NO2. It is a white crystalline solid that is soluble in water and various organic solvents. 2-Pyridinemethanol, a-(4-hydroxyphenyl)- is characterized by the presence of a pyridine ring (a six-membered aromatic ring containing one nitrogen atom) and a phenol group (a hydroxyl group attached to a benzene ring). It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Due to its unique structure, it exhibits interesting chemical properties and reactivity, making it a valuable compound in the field of organic chemistry and drug development.

33455-95-7

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33455-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33455-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,5 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33455-95:
(7*3)+(6*3)+(5*4)+(4*5)+(3*5)+(2*9)+(1*5)=117
117 % 10 = 7
So 33455-95-7 is a valid CAS Registry Number.

33455-95-7Relevant academic research and scientific papers

The light-emitting compound and use this light-emitting compound of the organic light emitting diode device

-

, (2017/04/11)

An embodiment of the present invention provides an emitting compound of following formula: wherein “A” is represented by and “B” is represented by

Synthesis of triphenylmethane derivative: Bisacodyl

Mereyala, Hari Babu,Sambaru, Kalyani

, p. 615 - 617 (2007/10/03)

A new method for the synthesis of bisacodyl 1 is described. The key step involves migration of 2-pyridacyl group of phenyl pyridine-2-carboxylate 4 in AlCl3 at 160 °C to yield the intermediate 4-hydroxyphenyl (2-pyridyl) ketone 5a. The reaction of 5a with phenol using H3PO 4 gives 1. This method has advantage over the existing literature methods because easily available pyridine-2-carboxylic acid is used as a starting material instead of the less stable pyridine-2-carboxaldehyde.

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