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2-((naphthalen-2-yl)methyl)phenol is an organic compound characterized by its molecular formula C17H14O. It features a phenol group (C6H5OH) with a naphthalene ring (C10H8) attached to the 2-position of the phenol through a methylene bridge (-CH2-). This chemical structure endows the compound with unique properties, such as its potential use as a building block in the synthesis of more complex organic molecules, including pharmaceuticals and other specialty chemicals. The compound's specific arrangement of aromatic rings and the presence of a hydroxyl group make it a versatile intermediate in organic synthesis, capable of undergoing a range of chemical reactions, such as oxidation, reduction, and substitution.

68299-60-5

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68299-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68299-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,9 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 68299-60:
(7*6)+(6*8)+(5*2)+(4*9)+(3*9)+(2*6)+(1*0)=175
175 % 10 = 5
So 68299-60-5 is a valid CAS Registry Number.

68299-60-5Relevant academic research and scientific papers

Synthesis of polycyclic xanthenes and furans via palladium-catalyzed cyclization of polycyclic aryltriflate esters

Wang, Ji-Quan,Harvey, Ronald G

, p. 5927 - 5931 (2002)

Palladium-catalyzed cyclization of polycyclic aromatic o-(arylmethyl)phenol triflate esters takes place with unexpected sulfur-oxygen bond cleavage to furnish polycyclic xanthenes. These are the first examples of Pd-catalyzed cross-coupling of aryl triflate esters with arenes to form diaryl ethers. In contrast, analogous palladium-catalyzed cyclization of polycyclic o-(aryloxy)phenol triflate esters proceeds via a mechanism that involves conventional carbon-oxygen bond cleavage to furnish diaryl furans.

4,4′-Unsymmetrically substituted 3,3′-biphenyl alpha helical proteomimetics as potential coactivator binding inhibitors

Weiser, Patrick T.,Chang, Ching-Yi,McDonnell, Donald P.,Hanson, Robert N.

, p. 917 - 926 (2014/01/23)

A series of unsymmetrically substituted biphenyl compounds was designed as alpha helical proteomimetics with the aim of inhibiting the binding of coactivator proteins to the nuclear hormone receptor coactivator binding domain. These compounds were synthes

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