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1,1,2-Triphenyl-2-propanol is an organic compound with the chemical formula C25H22O. It is a colorless, crystalline solid that is soluble in organic solvents. 1,1,2-triphenyl-2-propanol is characterized by a unique structure, featuring a propanol group (a three-carbon alcohol) with three phenyl rings (C6H5) attached to the second carbon. It is synthesized through various chemical reactions, such as the reduction of 1,1,2-triphenyl-2-propanone using sodium borohydride or lithium aluminum hydride. 1,1,2-Triphenyl-2-propanol has potential applications in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds due to its versatile structure and reactivity.

3677-79-0

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3677-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3677-79-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3677-79:
(6*3)+(5*6)+(4*7)+(3*7)+(2*7)+(1*9)=120
120 % 10 = 0
So 3677-79-0 is a valid CAS Registry Number.

3677-79-0Relevant academic research and scientific papers

Friedel-Crafts alkylation of benzene with 1,2-diphenyl-2-propanol, 1-chloro-2,3-diphenylpropane and 2-methyl-1-phenyl-2-butanol

Khalaf, Ali A.,Awad, Ibrahim M.,El-Emary,El-Aal, H.A.K. Abd

experimental part, p. 595 - 600 (2011/08/21)

The alkylation of benzene with 1,2-diphenyl-2-propanol (1) using AlCl 3/CH3NO2 catalyst gave a mixture of 1,2,2- (4) and 1,1,2-triphenylpropane (5) as product alkylates. With 85% H 2SO4 catalyst, the product consisted of E-1,2-diphenylpropene (6) after 2 h of a mixture of 5 and 6 after 18 h. Similar alkylation of benzene with 1-chloro-2,3-diphenylpropane (2) using AlCl 3 catalyst gave a mixture consisting of 4, 5 and 6. Finally, alkylation of benzene with 2-methyl-1-phenyl-2-butanol (3) using AlCl 3/CH3NO2 gave 2-methyl-1,1-diphenylbutane (10) as sole product alkylate. The identities of the products were confirmed spectroscopically and by comparison with unequivocally prepared samples. Mechanisms are proposed to rationalise the observed results.

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