110808-51-0 Usage
Bicyclic Compound
Yes
Explanation
The compound has two carbon atoms in a bridgehead position, which means it is composed of two rings connected by a single carbon-carbon bond.
Explanation
The compound appears as a colorless liquid, which means it does not have any distinct color when in its pure form.
Explanation
The molecular weight is the mass of one mole of a substance, and in this case, it is 144.17 grams per mole.
Explanation
The compound is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique structure and properties also make it a potential candidate for further research in the development of new materials and catalysts.
Explanation
The specific uses and applications of 1,1-Bicyclopropyl,2,2-difluoro-1,1-dimethyl-(9CI) may differ based on its particular characteristics and properties, which can be determined through further research and experimentation.
Fluorine Atoms
Two
Color
Colorless liquid
Molecular Weight
144.17 g/mol
Applications
Pharmaceutical and agrochemical synthesis, potential research in new materials and catalysts
Specific Uses
Vary depending on the specific characteristics and properties of the compound
Check Digit Verification of cas no
The CAS Registry Mumber 110808-51-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,0 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110808-51:
(8*1)+(7*1)+(6*0)+(5*8)+(4*0)+(3*8)+(2*5)+(1*1)=90
90 % 10 = 0
So 110808-51-0 is a valid CAS Registry Number.
110808-51-0Relevant academic research and scientific papers
REACTION OF DIFLUOROCARBENE WITH SMALL BICYCLIC MOLECULES
Jackson, E. James,Misslitz, Ulf,Jones, Maitland,Meijere, A. de
, p. 653 - 662 (2007/10/02)
Difluorocarbene reacts with 1,2,2-trimethylbicyclobutane to give the product of two bond cleavage, 1,1-difluoro-3,3,4-trimethyl-1,4-pentadiene in 3percent yield.Bicyclopentane is even less reactive, yielding 1,1-difluorohexa-1,5-diene in ca. 0.5percent yield.Bicyclohexane does not react with difluorocarbene.Theoretical descriptions of these reactions are discussed.
