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2,6-di-tert-butyl-4-(5-phenyl-[1,3,4]oxadiazol-2-yl)-phenol is a complex organic compound characterized by its molecular structure. It features a phenol core with two tert-butyl groups at the 2 and 6 positions, providing steric hindrance and stability. A 5-phenyl-[1,3,4]oxadiazol-2-yl group is attached at the 4 position, which contributes to the compound's electronic properties and potential applications. This chemical is known for its antioxidant properties and is often used as a stabilizer in industrial processes, particularly in the polymer and rubber industries, to prevent degradation caused by heat, light, and oxygen. Its unique structure also makes it a subject of interest in materials science and chemical research for potential applications in various fields.

3202-95-7

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3202-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3202-95-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,0 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3202-95:
(6*3)+(5*2)+(4*0)+(3*2)+(2*9)+(1*5)=57
57 % 10 = 7
So 3202-95-7 is a valid CAS Registry Number.

3202-95-7Downstream Products

3202-95-7Relevant academic research and scientific papers

Synthesis of 2,5-disubstituted 1,3,4-oxadiazoles containing a sterically hindered 4-hydroxy-3,5-di(tert-butyl)phenyl group

Kelarev,Koshelev,Silin

, p. 718 - 723 (1997)

A series of 2,5-disubstituted 1,3,4-oxadiazoles containing one or two 4-hydroxydi(tert-butyl)phenyl groups has been synthesized. These sterically hindered compounds were prepared by condensation of acids containing the indicated fragment and their derivatives with hydrazine dihydrochloride, hydrazides, and hydrochlorides of iminoesters of acids, by the reaction of 4-hydroxy-3,5-di(tert-butyl)thiphenol with 2-chloromethylsubstituted 1,3,4-oxadiazoles in the presence of KOH, and by cyclodehydration of N-acyl-N′-[4-hydroxy-3,5-di(tert-butyl)benzoyl]hydrazones under action of POCl3. 1997 Plenum Publishing Corporation.

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