696-84-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 4 carbon atoms, 2 chlorine atoms, 1 fluorine atom, and 3 nitrogen atoms.
Explanation
Triazine is a heterocyclic organic compound with a ring structure consisting of three nitrogen atoms and three carbon atoms. The compound belongs to this family.
Explanation
The compound has two chlorine atoms attached to the 2nd and 4th carbon atoms and one fluorine atom attached to the 6th carbon atom in the triazine ring.
Explanation
A heterocyclic compound is a cyclic compound containing atoms of at least two different elements. In this case, the triazine ring contains carbon and nitrogen atoms.
Explanation
The compound is used as a building block in the synthesis of various pharmaceuticals and agrochemicals due to its ability to form important chemical bonds and its versatile reactivity.
Explanation
It is also used as a precursor in the production of dyes, polymers, and other industrial chemicals, highlighting its diverse applications in the chemical industry.
Explanation
The triazine ring in the compound is aromatic, which means it has a planar structure and exhibits resonance stabilization.
Explanation
Although not explicitly mentioned, most organic compounds with similar molecular structures are solids at room temperature.
Explanation
The compound's reactivity is versatile, allowing it to form important chemical bonds and be used in various chemical reactions.
Explanation
As a chemical compound, it may have hazardous properties depending on its reactivity, toxicity, and other factors. However, this information is not provided in the material.
Chemical Family
Triazine
Substitution
2,4-dichloro-6-fluoro
Heterocyclic Compound
Yes
Building Block
Pharmaceutical and Agrochemical Synthesis
Precursor
Dyes, Polymers, and Industrial Chemicals
Chemical Structure
Aromatic
Physical State
Likely solid at room temperature
Reactivity
Versatile
Hazardous Nature
Potentially hazardous (not specified in the material)
Check Digit Verification of cas no
The CAS Registry Mumber 696-84-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 696-84:
(5*6)+(4*9)+(3*6)+(2*8)+(1*4)=104
104 % 10 = 4
So 696-84-4 is a valid CAS Registry Number.
696-84-4Relevant academic research and scientific papers
Ionic liquids as media for nucleophilic flurination
Murray, Christopher B.,Sandford, Graham,Korn, Stewart R.
, p. 81 - 84 (2007/10/03)
The use of Room Temperature Ionic Liquids (RTILs) for a variety of halogen exchange (Halex) fluorination processes using alkali metal fluorides is assessed. Whilst fluorination of a range of halogenated substrates is possible in good yield, the utility of RTILs as reusable, inert media for such reactions is limited by the gradual decomposition of the RTIL in the presence of highly basic fluoride ion.
LES FLUORATIONS COMPAREES DES CHLOROPYRIMIDINES ET DE LA CHLORO-S-TRIAZINE
Hitzke,J.
, p. 385 - 402 (2007/10/02)
The fluorinations of tetrachloropyrimidine, 2,4,6-trichloropyrimidine and trichloro-s-triazine were carried out in sealed tubes with KF in presence of inert gas and then compared.The fluorinated derivatives C4FxClyN2 with x + y = 4, O - were investigated and compared; the molar yields were found to be always higher than 50percent in our experimental conditions.We compare with the fluorinations of 2,4 and 4,6-dichloropyrimidine.It is possible to obtain directlyin good proportions, such fluorinated derivatives as 5-chlorotrifluoropyrimidine, trifluoropyrimidine and others.At high temperature (4OO deg C for 16h), tetrachloropyrimidine, in presence of KF, gave products of pyrolysis and condensation such as the fluorinated derivatives of C6Cl6 and C5Cl5N: C6FCl5, C6F2Cl4... or C5FCl4N, C5F2Cl3N...
