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2,2'-Diethoxy-1,1'-biphenyl is an organic compound with the chemical formula C14H18O2. It is a colorless liquid at room temperature and is characterized by its symmetrical biphenyl structure, where each phenyl ring is substituted with an ethoxy group at the 2-position. 2,2'-diethoxy-1,1'-biphenyl is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in materials science, such as in the production of polymers and as a solvent in certain industrial processes. Due to its reactivity and the presence of functional groups, it is important to handle 2,2'-diethoxy-1,1'-biphenyl with care, following proper safety protocols.

7168-53-8

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7168-53-8 Usage

Physical State

Colorless solid at room temperature

Solubility

Insoluble in water, soluble in organic solvents

Main Uses

Heat transfer fluid due to its high boiling point and thermal stability
Production of fragrances, dyes, and plastics

Potential Applications

In pharmaceuticals
As a flame retardant

Safety Considerations

Handle with care as it may be harmful if swallowed or inhaled
Can cause skin irritation
These properties and content details provide an overview of the chemical, its characteristics, uses, potential applications, and safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 7168-53-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,6 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7168-53:
(6*7)+(5*1)+(4*6)+(3*8)+(2*5)+(1*3)=108
108 % 10 = 8
So 7168-53-8 is a valid CAS Registry Number.

7168-53-8Relevant academic research and scientific papers

Catalyst-Free Synthesis of O-Heteroacenes by Ladderization of Fluorinated Oligophenylenes

Feofanov, Mikhail,Akhmetov, Vladimir,Takayama, Ryo,Amsharov, Konstantin

, p. 5199 - 5203 (2021/02/21)

A novel catalyst-free approach to benzoannulated oxygen-containing heterocycles from fluorinated oligophenylenes is reported. Unlike existing methods, the presented reaction does not require an oxygen-containing precursor and relies on an external oxygen source, potassium tert-butoxide, which serves as an O2? synthon. The radical nature of the reaction facilitates nucleophilic substitution even in the presence of strong electron-donating groups and enables de-tert-butylation required for the complete annulation. Also demonstrated is the applicability of the method to introduce five-, six-, and seven-membered rings containing oxygen, whereas multiple annulations also open up a short synthetic path to ladder-type O-heteroacenes and oligodibenzofurans.

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