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[1,1'-Biphenyl]-2-ol, 3,5-bis(1,1-dimethylethyl)is a chemical compound characterized by its molecular formula C26H36O. It is a white crystalline solid that exhibits solubility in organic solvents while being insoluble in water. [1,1'-Biphenyl]-2-ol, 3,5-bis(1,1-dimethylethyl)is utilized in a variety of industrial applications and serves as a fundamental building block in the synthesis of other chemical compounds.

7001-04-9

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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.

Check Digit Verification of cas no

The CAS Registry Mumber 7001-04-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7001-04:
(6*7)+(5*0)+(4*0)+(3*1)+(2*0)+(1*4)=49
49 % 10 = 9
So 7001-04-9 is a valid CAS Registry Number.

7001-04-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-ditert-butyl-6-phenylphenol

1.2 Other means of identification

Product number -
Other names 2-phenyl-4,6-di-tert-butylphenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7001-04-9 SDS

7001-04-9Relevant academic research and scientific papers

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

Barton, Derek H. R.,Finet, Jean-Pierre,Gianotti, Charles,Halley, Frank

, p. 4483 - 4494 (2007/10/02)

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

Barton, Derek H. R.,Yadav-Bhatnagar, Neerja,Finet, Jean-Pierre,Khamsi, Jamal,Motherwell, William B.,Stanforth, Stephen P.

, p. 323 - 332 (2007/10/02)

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.

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