1813-18-9 Usage
Description
3,3,3-Trifluoro-2,2-bis(trifluoromethyl)propanoyl fluoride is a colorless, non-flammable liquid chemical compound with the molecular formula C6H3F12O2. It is known for its high reactivity and unique chemical properties, which make it a valuable fluorinating reagent in organic synthesis and a building block for the production of specialty chemicals and pharmaceuticals.
Uses
Used in Organic Synthesis:
3,3,3-Trifluoro-2,2-bis(trifluoromethyl)propanoyl fluoride is used as a fluorinating reagent for the synthesis of various organic compounds. Its high reactivity allows for the efficient incorporation of fluorine atoms into target molecules, which can significantly alter their properties and improve their performance.
Used in Specialty Chemicals Production:
3,3,3-TRIFLUORO-2,2-BIS(TRIFLUOROMETHYL)PROPANOYL FLUORIDE serves as a building block in the production of specialty chemicals, which are often used in various industries due to their unique properties. Its role in creating these chemicals is crucial for the development of innovative products and materials.
Used in Pharmaceutical Industry:
3,3,3-Trifluoro-2,2-bis(trifluoromethyl)propanoyl fluoride is used as a key intermediate in the synthesis of pharmaceuticals. Its unique properties contribute to the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemicals Production:
In the agrochemical industry, this compound is utilized in the production of various pesticides and other agricultural chemicals. Its reactivity and properties enable the creation of effective and targeted agrochemicals that can protect crops and enhance agricultural productivity.
Used in Specialty Polymers and Materials Manufacturing:
3,3,3-Trifluoro-2,2-bis(trifluoromethyl)propanoyl fluoride is also employed in the manufacture of specialty polymers and materials. Its unique chemical structure allows for the development of advanced materials with specific properties, such as high thermal stability, chemical resistance, or improved mechanical strength.
Safety Precautions:
It is important to handle 3,3,3-trifluoro-2,2-bis(trifluoromethyl)propanoyl fluoride with care, as it can cause skin and eye irritation and is harmful if inhaled or ingested. Proper safety measures, including the use of personal protective equipment and handling in well-ventilated areas, should be taken to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 1813-18-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,1 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1813-18:
(6*1)+(5*8)+(4*1)+(3*3)+(2*1)+(1*8)=69
69 % 10 = 9
So 1813-18-9 is a valid CAS Registry Number.
1813-18-9Relevant articles and documents
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Adcock,J.L. et al.
, p. 3271 - 3275 (1975)
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The thermal decomposition of perfluoroesters [9]
Murata,Kawa,Lagow
, p. 7117 - 7118 (1998)
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Aerosol Direct Fluorination Syntheses: Alkyl Halides, Neopentyl Chloride and Bromide, Free Radicals vs. Carbocations
Adcock, James L.,Evans, William D.,Heller-Grossman, Lilly
, p. 4953 - 4957 (2007/10/02)
Aerosol direct fluorination of neopentyl chloride produces perfluoroneopentyl chloride in 74percent yields.Analogous fluorination of neopentyl bromide produces perfluoroisopentane in 63percent yield.Data are presented that support a carbocation rearrangement in the fluorination of neopentyl bromide.The carbocations are presumed to arise from disproportionation of neopentylbromine fluorides.
REACTIONS OF BIS(TRIFLUOROMETHYL)CARBAMOYL FLUORIDE WITH NUCLEOPHILIC REAGENTS
Gontar, A. F.,Bykhovskaya, E. G.,Vinogradov, A. S.,Knunyants, I. L.
, p. 2188 - 2191 (2007/10/02)
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