7001-04-9

Usage

Uses

Used in Pharmaceutical Industry:
[1,1'-Biphenyl]-2-ol, 3,5-bis(1,1-dimethylethyl)is used as a precursor in the production of pharmaceuticals, playing a crucial role in the development of various medications due to its unique chemical properties.
Used in Chemical Synthesis:
[1,1'-Biphenyl]-2-ol, 3,5-bis(1,1-dimethylethyl)is used as a reagent in organic synthesis, contributing to the creation of a wide range of chemical products.
Used in Polymer Manufacturing:
[1,1'-Biphenyl]-2-ol, 3,5-bis(1,1-dimethylethyl)is employed in the manufacturing of polymers, where it serves as a vital component in the production process.
Used in Plastics and Rubbers Industry:
It is also used as a stabilizer in the production of plastics and rubbers, enhancing the durability and performance of these materials.
Safety Considerations:
Although [1,1'-Biphenyl]-2-ol, 3,5-bis(1,1-dimethylethyl)is considered to have low toxicity, it is essential to adhere to proper handling and storage procedures to minimize any potential risks associated with its use.

Upstream product

• 732-26-3 2,4,6-tri-tert-butylphenoxol 
• 96-76-4 2,4-di-tert-Butylphenol 
• 28719-46-2 triphenylbismuth bis(trifluoroacetate) 
• 507-20-0 tertiary butyl chloride 
• 90-43-7 2-Phenylphenol 
• 107-39-1 2,4,4-trimethyl-1-pentene 

Downstream Products

• 103568-41-8 4-tert-Butyl-2,4-bis-(3,5-di-tert-butyl-biphenyl-2-yloxy)-6-phenyl-cyclohexa-2,5-dienone 
• 482683-70-5 (C₅H₅)Zr(OC₆H₂(C(CH₃)3)2C₆H₅)(CH₂C₆H₅)2 
• 151900-75-3 Ti(OC₆H₂(C(CH₃)3)2C₆H₅)2(N(CH₃)2)2 
• 151928-62-0 W₂(OC₆H₂(C(CH₃)3)2C₆H₅)2(N(CH₃)2)4 
• 151900-76-4 Nb(OC₆H₂(C(CH₃)3)2C₆H₅)2(N(CH₃)2)3 
• 138694-77-6 {Sn(OC₆H₂(C(CH₃)3)2C₆H₅)2(N(CH₃)2)2} 
• 97656-41-2 4-Phenyl-benzoesaeure-<2-phenyl-4,6-di-tert-butyl-phenyl>-ester 
• 98332-62-8 Biphenyl-(2-hydroxy-3-phenyl-5-tert-butyl-phenyl)-keton 
• 96113-95-0 benzoic acid-(3,5-di-tert-butyl-biphenyl-2-yl ester) 
• 98274-23-8 2-Phenyl-4-tert.-butyl-6-benzoyl-phenol 
• 97157-22-7 4-Nitrobenzoesaeure-(2-phenyl-4,6-di-tert-butyl-phenyl)-ester 
• 96972-38-2 <1,3-Di-tert.-butyl-5-phenyl-4-oxo-cyclohexadienyl>-<2,4,6-tri-phenyl-phenyl>-ether 

Relevant academic research and scientific papers

THE CHEMISTRY OF PENTAVALENT ORGANOBISMUTH REAGENTS. PART XI. REACTIONS WITH STERICALLY HINDERED PHENOLS.

The reactivity of BiV reagents towards very hindered phenols with tert.-butyl groups at 2 and 6 under basic conditions has been studied.Unexpected phenylation at the 4-position and, in several cases, replacement of a tert.-butyl group by phenyl have been observed.The mechanism of these unexpected reactions has been discussed.

THE CHEMISTRY OF PENTAVALENT ORGANOBISMUTH REAGENTS. PART X. STUDIES ON THE PHENYLATION AND OXIDATION OF PHENOLS

The influence of the substituents on the phenol on the regiochemistry of the arylation reactions with Ph3BiCl2 and other bismuth reagents has been studied.O-Phenylation occurs with phenols substituted with electron-withdrawing groups.Electron-donating substituted phenols undergo ortho C-phenylation.Oxidative dimerisation has been observed with 2,6-dialkyl phenols.