696-85-5 Usage
Chemical structure
A heterocyclic compound with a six-membered ring containing three nitrogen atoms and three carbon atoms, with one chlorine atom at the 2nd position, and two fluorine atoms at the 4th and 6th positions.
Functional groups
Chlorine (Cl), Fluorine (F), and triazine ring.
Physical state
Likely a solid at room temperature, based on its molecular weight and structure.
Applications
a. Building block for pharmaceuticals, agrochemicals, and specialty chemicals.
b. Intermediate in the production of herbicides, insecticides, and fungicides.
c. Reagent in organic synthesis for the preparation of heterocyclic compounds and complex chemical structures.
d. Potential applications in materials science and polymer chemistry.
Properties
a. Potent inhibitor of microbial growth.
b. Versatile reactivity and functional group compatibility.
Hazards
Not mentioned in the provided material, but it is important to consider potential hazards and safety precautions when handling 1,3,5-Triazine, 2-chloro-4,6-difluoro-, as it may be toxic or harmful depending on its concentration and exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 696-85-5 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 696-85:
(5*6)+(4*9)+(3*6)+(2*8)+(1*5)=105
105 % 10 = 5
So 696-85-5 is a valid CAS Registry Number.
696-85-5Relevant 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...
