1619-92-7 Usage
Uses
Used in Pharmaceutical Synthesis:
1,1,1,3,3,3-Hexafluoroisopropylamine is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs with improved properties such as enhanced bioavailability and targeted delivery.
Used in Agrochemical Production:
In the agrochemical industry, 1,1,1,3,3,3-Hexafluoroisopropylamine serves as a key component in the creation of pesticides and other crop protection agents, aiming to increase the effectiveness and selectivity of these products.
Used in Specialty Chemicals:
1,1,1,3,3,3-Hexafluoroisopropylamine is utilized as a precursor in the production of specialty chemicals, which are tailored for specific applications in various industries, such as coatings, adhesives, and sealants.
Used as a Solvent:
HFI is employed as a solvent in certain chemical processes, taking advantage of its unique properties to dissolve a range of substances and facilitate reactions.
Used as a Reagent in Organic Reactions:
In organic chemistry, 1,1,1,3,3,3-Hexafluoroisopropylamine functions as a reagent, participating in various reactions to form desired products or to modify the properties of existing compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1619-92-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1619-92:
(6*1)+(5*6)+(4*1)+(3*9)+(2*9)+(1*2)=87
87 % 10 = 7
So 1619-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H3F6N/c4-2(5,6)1(10)3(7,8)9/h1H,10H2
1619-92-7Relevant academic research and scientific papers
REACTION OF INTERNAL PERFLUORINATED α-OXIDES WITH AMMONIA
Saloutina, L. V.,Zapevalov, A. Ya.,Kodess, M. I.,Kolenko, I. P.
, p. 628 - 634 (2007/10/02)
The action of ammonia leads to nucleophilic opening of the epoxide ring in internal perfluorinated α oxides with the formation of aminoiminoperfluoroalkanols and their dissociation products.In unsymmetrical disubstituted 2,3-epoxyperfluoroalkanes attack by ammonia at the carbon atoms of the epoxide ring is not regioselective, whereas in the trisubstituted compounds regiospecific reaction with ammonia occurs.The stability of the internal perfluorinated α-oxides to the action of ammonia is increased with increase in the size of the fluoroalkyl substituents.
An Unexpected Reaction of Diphenyldiazomethane with Perfluoro-2-nitrosopropane
Banks, Ronald Eric,Richards, Adrian
, p. 205 - 206 (2007/10/02)
Diphenyldiazomethane reacts with perfluoro-2-nitrosopropane at low temperatures to yield the oxime ether (CF3)2C=NOCFPh2, some chemistry of which has been explored.
