1482-03-7 Usage
Explanation
The compound consists of 7 carbon atoms, 6 hydrogen atoms, and 6 fluorine atoms.
Explanation
The compound has two interconnected rings, forming a bicyclic structure.
Explanation
The compound appears as a colorless liquid under normal temperature conditions.
Explanation
It is mainly used as a starting material for the production of various drugs and agricultural chemicals.
Explanation
The compound is also utilized as a solvent in various chemical processes.
Explanation
Due to its chemical structure, the compound is very reactive and can easily participate in chemical reactions.
Explanation
The compound should be handled with care due to its potential to cause harm to human health and its ability to burn or ignite.
Explanation
Special care should be taken when working with this compound to minimize the risk of accidents or exposure to harmful effects.
Bicyclic structure
Yes
Fluorine atom positions
1, 2, 3, 4, 7, and 7
Physical state at room temperature
Colorless liquid
Primary use
Intermediate in the synthesis of pharmaceuticals and agrochemicals
Secondary use
Solvent in the chemical industry
Reactivity
Highly reactive
Safety concerns
Potential health hazards and flammability
Precautions
Handle with care
Check Digit Verification of cas no
The CAS Registry Mumber 1482-03-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1482-03:
(6*1)+(5*4)+(4*8)+(3*2)+(2*0)+(1*3)=67
67 % 10 = 7
So 1482-03-7 is a valid CAS Registry Number.
1482-03-7Relevant articles and documents
Extremely facile ring inversion and rearrangement in fluorobicyclo[2.1.0]pentanes
Wei, Yanjun,Liu, Yufa,Wong, Terrence,Lemal, David M.
, p. 688 - 703 (2008/09/16)
cis-1,2,3,4,5,5-Hexafluorobicyclo[2.1.0]pentane and 1,2,4,5-tetrafluorobicyclo[2.1.0]pentane have been synthesized from hexafluorobenzene. The former hydrofluorocarbon, which exists entirely in the endo configuration, rearranges to cis-1,2,3,3,4,5-hexafluorocyclopentene below room temperature (Ea = 21.9 kcal/mol, log A = 13.4). The latter undergoes degenerate ring inversion with extraordinary ease (ΔG? = 6.8 ± 0.2 kcal/mol at -55 °C). Density functional calculations indicate that significant bonding between the bridgehead carbons is retained in the ring inversion transition state. Analogous calculations predict for hexafluorobicyclo[1.1.0]butane a considerably lower barrier for ring inversion and more 1,3-bonding in the transition state.
