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α-cyclohexyl-α-phenyl-2-pyridinemethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109253-36-3

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109253-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109253-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,2,5 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109253-36:
(8*1)+(7*0)+(6*9)+(5*2)+(4*5)+(3*3)+(2*3)+(1*6)=113
113 % 10 = 3
So 109253-36-3 is a valid CAS Registry Number.

109253-36-3Downstream Products

109253-36-3Relevant academic research and scientific papers

Green synthesis method of polyaryl substituted methanol

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Paragraph 0127-0131; 0317-0321, (2021/04/17)

The invention relates to a green synthesis method of polyaryl substituted methanol, in particular to a method for efficiently synthesizing polyaryl substituted methanol in a polar aprotic solvent under the condition of an oxidizing agent by taking polyaryl substituted methane as a raw material and alkali as an additive. The method provided by the invention is green and environment-friendly, avoids using expensive metal catalysts, and has the advantages of low cost, few reaction steps, short time, high yield and the like.

Transition-Metal Free Chemoselective Hydroxylation and Hydroxylation-Deuteration of Heterobenzylic Methylenes

Fu, Yiwei,Li, Hao,Liu, Yonghai,Mang, Zhiguo,Shi, Lei,Sun, Chengyu,Yu, Yang

, p. 8127 - 8131 (2020/11/03)

We developed an approach for direct selective hydroxylation of heterobenzylic methylenes to secondary alcohols avoiding overoxidation to ketones by using a KOBu-t/DMSO/air system. Most reactions could reach completion in several minutes to give hydroxylated products in 41-76% yields. Using DMSO-d6, this protocol resulted in difunctionalization of heterobenzylic methylenes to afford α-deuterated secondary alcohols (>93% incorporation). By employing this method, active pharmaceutical ingredients carbinoxamine and doxylamine were synthesized in two steps in moderate yields.

[1,2]-Anionic rearrangement of 2-benzyloxypyridine and related pyridyl ethers

Yang, Jingyue,Dudley, Gregory B.

supporting information; experimental part, p. 7998 - 8000 (2010/03/01)

(Chemical Equation Presented) An anionic rearrangement of 2-benzyloxypyridine is described. Pyridine-directed metalation of the benzylic carbon leads to 1,2-migration of pyridine via a postulated associative mechanism (addition/elimination). Several aryl pyridyl carbinols were obtained in high yields. A formal synthesis of carbinoxamine, an antihistamine drug used for the treatment of seasonal allergies and hay fever, emerges from this methodology.

Method of regulating the growth of aquatic weeds with pyridine derivatives

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, (2008/06/13)

A method of regulating the growth of submerged and floating aquatic weeds which comprises adding a 2- or 4-substituted pyridinemethane or pyridinemethanol to a body of water containing the submerged and floating aquatic weeds to be regulated, in quantities sufficient to regulate the growth of the submerged and floating aquatic weeds therein. The disclosure also relates to novel compositions for carrying out the method.

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