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Phenol, 4-(2-benzoxazolyl)-2,6-bis(1,1-dimethylethyl)-, also known as 2,6-di-tert-butyl-4-(2-benzoxazolyl)phenol, is a complex organic compound with the chemical formula C22H25NO2. It is a derivative of phenol, featuring a benzoxazole group attached to the 4-position and two tert-butyl groups at the 2 and 6 positions. Phenol, 4-(2-benzoxazolyl)-2,6-bis(1,1-dimethylethyl)- is characterized by its white crystalline appearance and is soluble in organic solvents. It is primarily used as an antioxidant in various industrial applications, such as in the stabilization of polymers and plastics, to prevent oxidative degradation and extend their service life. Due to its chemical structure, it exhibits excellent thermal and UV stability, making it a valuable additive in the manufacturing of materials that require resistance to heat and light exposure.

3202-91-3

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3202-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3202-91-3 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 3202-91:
(6*3)+(5*2)+(4*0)+(3*2)+(2*9)+(1*1)=53
53 % 10 = 3
So 3202-91-3 is a valid CAS Registry Number.

3202-91-3Relevant academic research and scientific papers

PRODUCTION METHOD OF 2-(HYDROXYPHENYL) BENZOXAZOLES

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Paragraph 0037, (2016/12/07)

PROBLEM TO BE SOLVED: To provide a production method of 2-(hydroxyphenyl) benzoxazoles. SOLUTION: A method of producing 2-(hydroxyphenyl) benzoxazoles is characterized by reacting a 2-nitro phenol compound having, in a molecule, at least one a benzene ring substituted with a hydroxyl group at one and a nitro group at the other of mutually adjacent carbon atoms or a condensed polycyclic hydrocarbon ring comprising the benzene ring, with a methyl phenol compound having a benzene ring substituted with a methyl group and a hydroxyl group. COPYRIGHT: (C)2015,JPOandINPIT

Redox-neutral iron-sulfur promoted transformation of 2-nitrophenols and 2,6-disubstituted p -cresols into 2-arylbenzoxazoles

Saibara, Masahiko,Ashida, Kazuhito,Satomi, Kouji,Iwai, Toshiyuki,Nakai, Takeo,Mihara, Masatoshi,Ito, Takatoshi,Mizuno, Takumi

supporting information, p. 1565 - 1570 (2014/07/08)

A catalyst based on iron and elemental sulfur has been shown to efficiently promote a redox-neutral reaction between 2-nitrophenols and 2,6-disubstituted p-cresols, allowing for the preparation of 2-arylbenzoxazoles in good yields. This synthetic methodology also affords high atom economy without the use of any external oxidizing and/or reducing reagents. This is the first redox-condensation reaction of 2-nitrophenols with 2,6-disubstituted p-cresols. Georg Thieme Verlag Stuttgart New York.

SYNTHESIS AND PROPERTIES OF AZOLES AND THEIR DERIVATIVES. 35. SYNTHESIS OF CERTAIN AZOLES CONTAINING STERICALLY HINDERED PHENOL RESIDUES

Kelarev, V. I.,Shvekhgeimer, S. G.,Koshelev, V. N.,Shvekhgeimer, G. A.,Lunin, A. F.

, p. 721 - 723 (2007/10/02)

The condensation of hydrochlorides of ethyl iminoesters of 4-hydroxy-3,5-di-tert-butylbenzoic and β-(4-hydroxy-3,5-di-tert-butylphenyl)propionic acids with monoethanolamine, o-aminophenol, and o-phenylenediamine was studied.As a result, Δ2-oxaz

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