5002-42-6 Usage
Structure
Ketone derivative with a biphenyl structure
The molecule contains a carbonyl group (C=O) and a biphenyl group, which consists of two connected phenyl rings.
Fluorine substitution
Attached to the 3' position of the biphenyl structure
The fluorine atom is located at the 3' position, which is the meta position relative to the carbonyl group on the biphenyl.
Applications
Building block in organic synthesis and chemical research
The compound serves as a starting material for the synthesis of various organic compounds with diverse functionalities.
Potential uses
Pharmaceuticals, agrochemicals, and materials science
Due to its unique structure and properties, the compound has potential applications in the development of new drugs, agrochemicals, and advanced materials.
Synthetic intermediate
Utilized to prepare a variety of organic compounds
As a synthetic intermediate, 1-(3'-fluoro-biphenyl-4-yl)-ethanone can be used to create a wide range of organic compounds with different applications.
Physical properties
Not provided in the material
The material does not provide information about the physical properties of the compound, such as melting point, boiling point, or solubility.
Chemical properties
Not provided in the material
The material does not provide information about the chemical properties of the compound, such as reactivity, stability, or functional group behavior.
Check Digit Verification of cas no
The CAS Registry Mumber 5002-42-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5002-42:
(6*5)+(5*0)+(4*0)+(3*2)+(2*4)+(1*2)=46
46 % 10 = 6
So 5002-42-6 is a valid CAS Registry Number.
5002-42-6Relevant academic research and scientific papers
Formation Constants of Cyanohydrins of Substituted Acetylbiphenyls
Ananthakrishnanadar, P.,Kannan, N.
, p. 74 - 75 (2007/10/02)
The formation constants of cyanohydrins of 2'- and 3'-substituted 4-acetylbiphenyls have been determined at 30 deg C in 80percent dioxan-water (v/v).The 3'-substituted 4-acetylbiphenyls obey the Hammett equation giving a ρ-value of 0.52; 2'-substituted cyanohydrins do not obey the Hammett equation.The formation constants of 3'-substituted 4-acetylbiphenyls and their rate constants for the reduction by sodium borohydride reveal a linear relationship (r = 0.990).The influence of 2'-substituents reveals the existence of ?-electron steric effect.
