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[1,1':3',1''-Terphenyl]-2'-ol, 5'-(1,1-dimethylethyl)-, also known as 2'-hydroxy-5'-tert-butylterphenyl, is an organic compound with the molecular formula C21H24O. It is a derivative of terphenyl, a type of polycyclic aromatic hydrocarbon, and features a hydroxyl group at the 2' position and a tert-butyl group at the 5' position. [1,1':3',1''-Terphenyl]-2'-ol, 5'-(1,1-dimethylethyl)- is characterized by its symmetrical structure and is often used as a reference material in various chemical and physical studies due to its well-defined structure and properties. It is also relevant in the field of materials science, particularly in the study of polymers and organic semiconductors, where its electronic and steric properties can influence material behavior.

6863-52-1

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6863-52-1 Usage

Uses

Used in Organic Synthesis:
[1,1':3',1''-Terphenyl]-2'-ol, 5'-(1,1-dimethylethyl)is used as a building block in organic synthesis for creating new compounds with specific properties and applications. Its unique structure and functional groups allow for the development of a wide range of chemical products.
Used in Research Applications:
In the field of research, [1,1':3',1''-Terphenyl]-2'-ol, 5'-(1,1-dimethylethyl)serves as a valuable tool for studying the properties and behavior of terphenyl derivatives. It can be used to investigate various chemical reactions and interactions, contributing to the advancement of scientific knowledge in this area.
Used in Industrial Applications:
[1,1':3',1''-Terphenyl]-2'-ol, 5'-(1,1-dimethylethyl)is also utilized in various industrial applications, where its unique structure and functional groups can be harnessed to create compounds with specific uses. These applications may include the development of materials for electronics, pharmaceuticals, or other specialized industries.
Used in Pharmaceutical Development:
In the pharmaceutical industry, [1,1':3',1''-Terphenyl]-2'-ol, 5'-(1,1-dimethylethyl)can be used as a starting material for the synthesis of novel drug candidates. Its unique structure and functional groups may contribute to the development of new medications with improved efficacy and reduced side effects.
Used in Material Science:
In material science, [1,1':3',1''-Terphenyl]-2'-ol, 5'-(1,1-dimethylethyl)may be employed in the development of advanced materials with specific properties, such as improved conductivity, stability, or other desired characteristics. Its unique structure and functional groups can be tailored to meet the needs of various applications in this field.

Check Digit Verification of cas no

The CAS Registry Mumber 6863-52-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,6 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6863-52:
(6*6)+(5*8)+(4*6)+(3*3)+(2*5)+(1*2)=121
121 % 10 = 1
So 6863-52-1 is a valid CAS Registry Number.

6863-52-1Relevant academic research and scientific papers

Pseudocyclic Arylbenziodoxaboroles: Efficient Benzyne Precursors Triggered by Water at Room Temperature

Yoshimura, Akira,Fuchs, Jonathan M.,Middleton, Kyle R.,Maskaev, Andrey V.,Rohde, Gregory T.,Saito, Akio,Postnikov, Pavel S.,Yusubov, Mekhman S.,Nemykin, Victor N.,Zhdankin, Viktor V.

supporting information, p. 16738 - 16742 (2017/12/02)

New organohypervalent iodine compounds, arylbenziodoxaborole triflates, were prepared from 1-acetoxybenziodoxaboroles and arenes by treatment with trifluoromethanesulfonic acid under mild conditions. Single crystal X-ray crystallography of these compounds revealed a pseudocyclic structure with a short intramolecular interaction of 2.698 to 2.717 ? between oxygen and iodine in the benziodoxaborole ring. These new pseudocyclic aryliodonium salts readily generate aryne intermediates upon treatment with water at room temperature. The generated aryne intermediates react with various substrates to give the corresponding aryne adducts in moderate to good yields. Furthermore, the new benzyne precursors can also work as arylating reagents towards aromatic rings. The aryne intermediates generated from arylbenziodoxaborole triflates selectively react with tert-butyl phenol forming products of ortho arylation in moderate yields.

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