4040-29-3 Usage
Chemical Class
Biphenyl derivatives
Explanation
1,1'-Biphenyl, 4-ethenyl-4'-methylbelongs to the class of biphenyl derivatives, which are organic compounds consisting of two benzene rings linked by a single carbon-carbon bond.
Explanation
The compound is formed by connecting two benzene rings through a single bond between a carbon atom in each ring.
Explanation
The compound has an ethenyl (vinyl) group attached to the 4th carbon atom of one benzene ring and a methyl group attached to the 4th carbon atom of the other benzene ring.
Explanation
1,1'-Biphenyl, 4-ethenyl-4'-methylis utilized in various industrial processes and chemical synthesis, making it a valuable compound for the production of different organic compounds.
Explanation
Due to its chemical properties and potential uses, 1,1'-Biphenyl, 4-ethenyl-4'-methylattracts attention from researchers and industries that focus on creating innovative materials and products.
Explanation
The molecular formula of 1,1'-Biphenyl, 4-ethenyl-4'-methylindicates that it consists of 15 carbon atoms and 14 hydrogen atoms.
Explanation
The molecular weight of 1,1'-Biphenyl, 4-ethenyl-4'-methylis around 190.28 grams per mole, which is a measure of its mass in one mole of the compound.
Explanation
Although the exact physical state is not provided, most biphenyl derivatives are solids or liquids at room temperature, depending on their molecular structure and substituents.
Explanation
Biphenyl derivatives, including 1,1'-Biphenyl, 4-ethenyl-4'-methyl-, are generally soluble in organic solvents such as ethanol, acetone, and dichloromethane.
Explanation
1,1'-Biphenyl, 4-ethenyl-4'-methylis expected to be stable under normal conditions, such as room temperature and pressure, without undergoing significant decomposition or reaction.
Structure
Two benzene rings linked by a single carbon-carbon bond
Substituents
Ethenyl group at the 4th position on one benzene ring and a methyl group at the 4th position on the other benzene ring
Industrial Applications
Used in industrial processes and chemical synthesis
Research Interest
Of interest to researchers and industries involved in the development of new materials and products
Molecular Weight
Approximately 190.28 g/mol
Physical State
Likely a solid or liquid at room temperature
Solubility
Soluble in organic solvents
Stability
Stable under normal conditions
Check Digit Verification of cas no
The CAS Registry Mumber 4040-29-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,4 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4040-29:
(6*4)+(5*0)+(4*4)+(3*0)+(2*2)+(1*9)=53
53 % 10 = 3
So 4040-29-3 is a valid CAS Registry Number.
4040-29-3Relevant academic research and scientific papers
Preperations and Reactions of Symmetrical Dimethylenebiphenyl Dianions; Conformations of -o-Cyclophanes. A Simple NMR method for Determining Twist Angles in Biphenyls
Bates, Robert B.,Camou, Fernando A.,Kane, Vinayak V.,Mishra, Prasana K.,Suvannachut, Kessara,White, James J.
, p. 311 - 317 (2007/10/02)
With n-butyllithium / potassium tert-butoxide, a proton is removed from each methyl group of the symmetrical dimethylbiphenyls to give dianions in good yield.The reactions of these dianions with alkyl halides, dialkyl sulfates, trimethylchlorosilane, trimethylchlorogermane, α,ω-dihalides, and oxidizing agents were found to provide the best routes to many symmetrically substituted biphenyls, including - and cyclophanes.NMR and molecular mechanical studies of some of these cyclophanes gave information on their preferred conformations.An NMR method for determining the angle of twist in biphenyls from the chemical shifts of the ortho hydrogens is developed.
