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Phenol, 2,6-bis(1,1-dimethylethyl)-4-[(phenylimino)methyl]-, also known as 2,6-di-tert-butyl-4-(phenylimino)phenol, is a chemical compound with the molecular formula C22H25NO. It is a derivative of phenol, characterized by the presence of two tert-butyl groups (1,1-dimethylethyl) at the 2 and 6 positions, and a phenylimino group at the 4 position. Phenol, 2,6-bis(1,1-dimethylethyl)-4-[(phenylimino)methyl]- is often used as an antioxidant in various industrial applications, such as in the stabilization of polymers and lubricants, to prevent oxidative degradation. Its chemical structure provides it with the ability to scavenge free radicals, thereby protecting materials from the damaging effects of oxidation.

7313-26-0

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7313-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7313-26-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,1 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7313-26:
(6*7)+(5*3)+(4*1)+(3*3)+(2*2)+(1*6)=80
80 % 10 = 0
So 7313-26-0 is a valid CAS Registry Number.

7313-26-0Relevant academic research and scientific papers

Synthesis and medicinal properties of 4-benzylidene-1-phenyl-2-(substituted styryl)imidazolin-5-ones

Madhavi,Prasad,Bharathi

experimental part, p. 5588 - 5594 (2012/08/07)

A series of 4-benzylidene-1-phenyl-2-(substituted styryl)imidazolin-5-ones have been synthesized by the interaction of 4-benzylidene-2-methyloxazol-5-one with different Schiff bases, prepared by simple condensation of aniline and various substituted benzaldehydes. The title compounds were evaluated for antiinflammatory activity in carrageenan foot paw edema model and in vitro antioxidant activity. Among the 14 compounds synthesized, dimethyl amino derivative and sterically hindered phenolic derivatives were found to possess good antiinflammatory activity which also exhibited antioxidant properties.

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