6257-38-1

Usage

Uses

Used in Polymer and Plastics Industry:
[1,1'-Biphenyl]-4-ol, 3,5-bis(1,1-dimethylethyl)-4'-methylis used as a stabilizer in the production of polymers and plastics. Its antioxidant properties help prevent the degradation of these materials, thereby enhancing their durability and performance.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [1,1'-Biphenyl]-4-ol, 3,5-bis(1,1-dimethylethyl)-4'-methylis used as a starting material for the synthesis of various drugs. Its versatile chemical structure allows for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agricultural Industry:
[1,1'-Biphenyl]-4-ol, 3,5-bis(1,1-dimethylethyl)-4'-methylalso has potential applications in the agricultural industry. Its chemical structure and potential biological activities make it a candidate for the development of new agrochemicals, such as pesticides or plant growth regulators.
Used in Industrial and Consumer Product Manufacturing:
[1,1'-Biphenyl]-4-ol, 3,5-bis(1,1-dimethylethyl)-4'-methylis utilized as a stabilizer in the manufacturing of various industrial and consumer products. Its antioxidant properties help protect these products from degradation, ensuring their longevity and reliability.

Upstream product

• 59313-64-3 4-(4-Methyl-phenyl)-2,6-di-tert.-butyl-4-hydroxycyclohexadien-(2,5)-on 

Downstream Products

• 63406-96-2 2,6-Di-tert-butyl-6-hydroperoxy-4-p-tolyl-cyclohexa-2,4-dienone 
• 59313-64-3 4-(4-Methyl-phenyl)-2,6-di-tert.-butyl-4-hydroxycyclohexadien-(2,5)-on 
• 58281-55-3 2,5-Di-tert-butyl-3-p-tolyl-cyclopenta-2,4-dienone 
• 66475-75-0 2,6-Di-tert-butyl-4,5,6-trihydroxy-4-p-tolyl-cyclohex-2-enone 
• 62363-62-6 Co((CH₂)3NCHC₆H₄O)2NHOOC₆H₂(C(CH₃)3)2OC₆H₄CH₃ 
• 69217-47-6 2,6-Di-t-butyl-4-methoxy-4-(4-methylphenyl)-cyclohexadienon 

Relevant academic research and scientific papers

Novel Reduction of 2,6-Di-t-butyl-p-quinols with Sodium Borohydride

Reduction of 2,6-di-t-butyl-p-quinols with NaBH4 results unexpectedly in the regio- and stereoselective formation of the corresponding dihydro-p-quinols.The novel reduction occurs via a quinoxyborohydride anion intermediate, which regulates the stereochemistry of the 4- and 6-positions in the products.Aromatization of the products is blocked by the t-butyl groups.