116089-64-6 Usage
Chemical Structure
1H-Fluorene, 4,4a-dihydro-1,1,3-trimethyl-9-phenyl-
Explanation
This describes the specific arrangement of atoms and bonds in the molecule. The fluorene backbone has a phenyl group attached at the 9th position and methyl groups at the 1st and 3rd positions.
Explanation
Fluorene is a type of PAH, which are organic compounds consisting of multiple aromatic rings. 1H-Fluorene, 4,4a-dihydro-1,1,3-trimethyl-9-phenyl- is a derivative of fluorene, meaning it has a similar structure but with some modifications.
Explanation
The fluorene backbone consists of three fused aromatic rings, which contribute to its stability and chemical properties.
Explanation
The molecule has three methyl groups attached to the fluorene backbone and one phenyl group attached at the 9th position. These groups influence the compound's reactivity and properties.
Explanation
Due to its unique structural and chemical properties, 1H-Fluorene, 4,4a-dihydro-1,1,3-trimethyl-9-phenyl- is used as a building block for the preparation of other organic compounds and has potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
Explanation
Due to its nonpolar nature and the presence of carbon-hydrogen bonds, 1H-Fluorene, 4,4a-dihydro-1,1,3-trimethyl-9-phenyl- is expected to be soluble in organic solvents such as dichloromethane, ethyl acetate, or toluene.
Explanation
The presence of functional groups in the molecule allows it to undergo various chemical reactions, such as substitution, addition, or elimination reactions, to form new compounds.
Derivative of Fluorene
Polycyclic Aromatic Hydrocarbon (PAH)
Aromatic Rings
Three
Functional Groups
Methyl groups (-CH3) and a phenyl group (C6H5)
Applications
Organic Synthesis, Pharmaceutical, Agrochemical, and Materials Science
Stability
Relatively stable
Solubility
Likely soluble in organic solvents
Reactivity
Reacts with various reagents to form new compounds
Check Digit Verification of cas no
The CAS Registry Mumber 116089-64-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,8 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116089-64:
(8*1)+(7*1)+(6*6)+(5*0)+(4*8)+(3*9)+(2*6)+(1*4)=126
126 % 10 = 6
So 116089-64-6 is a valid CAS Registry Number.
116089-64-6Relevant academic research and scientific papers
PROPARGYL CATIONS--POWERFUL AMBIENT TEMPERATURE DIENOPHILES IN THE DIELS-ALDER REACTION
Gassman, Paul G.,Singleton, Daniel A.
, p. 5969 - 5972 (2007/10/02)
The diphenylpropargyl cation has been shown to be a powerful Diels-Alder dienophile which adds to dienes in high yield at ambient temperatures.
