393-05-5 Usage
Chemical structure
A benzene ring with three trifluoromethyl groups attached at the 1, 2, and 4 positions.
Physical state
Colorless liquid
Reactivity
High reactivity, commonly used as a starting material in organic reactions to introduce trifluoromethyl groups into various molecules.
Organic synthesis
Widely used in organic synthesis as a building block for the production of various pharmaceuticals, agrochemicals, and materials.
Medicinal chemistry
Has potential applications as an anti-inflammatory and anticancer agent.
Stability
Due to the presence of trifluoromethyl groups, the compound is relatively stable.
Solubility
Likely soluble in organic solvents due to its nonpolar nature.
Boiling point
Not provided, but can be inferred to be relatively high due to the presence of multiple fluorine atoms, which increase the intermolecular forces.
Density
Not provided, but can be inferred to be higher than water due to the presence of fluorine atoms, which are heavier than hydrogen atoms.
Check Digit Verification of cas no
The CAS Registry Mumber 393-05-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 393-05:
(5*3)+(4*9)+(3*3)+(2*0)+(1*5)=65
65 % 10 = 5
So 393-05-5 is a valid CAS Registry Number.
393-05-5Relevant articles and documents
Unusual reactivity of poly(trifluoromethyl)benzenes. Semiempirical reaction modelling
Koroinak, Henryk,Fiedorow, Piotr,Dmowski, Wojciech,Porwisiak, Jacek
, p. 187 - 196 (1995)
The reaction of methyllithium with 1,3,5-tris(trifluoromethyl)benzene, 1, 1,2,4,5-tetrakis(trifluoromethyl)benzene, 2, and 1,2,4-tris(trifluoromethyl)benzene, 3, was analyzed using the semiempirical package MOPAC 6.It was shown that formation of lithium-h
