116470-64-5 Usage
Appearance
Unknown, but likely a solid due to its molecular weight and structure
Explosive nature
Highly explosive
Toxicity
Highly toxic
Uses
Manufacturing of explosives, dyes, and pharmaceuticals
Reactivity
Extremely reactive and unstable
Nitro groups
Contains two nitro (-NO2) groups
Trifluoromethyl groups
Contains two trifluoromethyl (-CF3) groups
Regulation
Highly regulated due to its explosive and toxic nature
Handling and storage
Requires special handling and storage
Health effects
Can cause severe irritation of the respiratory system, skin, and eyes, as well as potential long-term damage to the liver and kidneys
Safety protocols
Must be handled and used with extreme caution and in accordance with strict safety protocols
Check Digit Verification of cas no
The CAS Registry Mumber 116470-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,7 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116470-64:
(8*1)+(7*1)+(6*6)+(5*4)+(4*7)+(3*0)+(2*6)+(1*4)=115
115 % 10 = 5
So 116470-64-5 is a valid CAS Registry Number.
116470-64-5Relevant articles and documents
Synthesis of trifluoromethyl aryl derivatives via difluorocarbene precursors and nitro-substituted aryl chlorides
Duan, Jian-Xing,Su, De-Bao,Wu, Jian-Ping,Chen, Qing-Yun
, p. 167 - 170 (1994)
Treatment of aryl chlorides containing electron-withdrawing proups with methyl fluorosulfonyl difluoroacetate or methyl halodifluoroacetate in the presence of potassium fluoride and copper iodide gave the corresponding trifluoromethyl derivatives in moderate to high yields.
THE TRIFLUOROMETHYLATION OF CHLOROAROMATICS USING THE COPPER-CF2Br2-DIALKYLAMIDE REACTION SYSTEM
Clark, James H.,Denness, James E.,McClinton, Martin A.,Wynd, Andrew J.
, p. 411 - 426 (2007/10/02)
The in situ generation of CuCF3 from the reaction of copper, dibromodifluoromethane and either N,N-dimethylformamide or N,N-dimethylacetamide (Burton's reagent) has been used for the direct substitution of chlorine by CF3 in a number of aromatic substrates.Particular attention has been paid to the effects of ring substituents on the efficiency of reaction.
