460-13-9 Usage
Uses
Used in Chemical Synthesis:
1-Fluoropropane is used as a reagent in the chemical synthesis industry for the production of various compounds. Its unique properties as a halogenated hydrocarbon make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Refrigeration:
1-Fluoropropane is used as a refrigerant in the refrigeration industry. Its low toxicity, high energy efficiency, and non-ozone-depleting characteristics make it an environmentally friendly alternative to traditional refrigerants. It is particularly useful in commercial and industrial refrigeration systems, as well as in air conditioning units.
Used in Propellant Applications:
1-Fluoropropane is used as a propellant in aerosol products, such as spray paints, deodorants, and other consumer goods. Its ability to create a fine mist and its low toxicity make it a preferred choice for these applications.
Used in Cleaning Agents:
1-Fluoropropane is used as a cleaning agent in the electronics and metal industries. Its ability to dissolve various types of residues and contaminants makes it an effective cleaning solution for delicate components and surfaces.
Used in Fire Suppression Systems:
1-Fluoropropane is used as a fire suppressant in fire protection systems. Its ability to rapidly reduce the oxygen concentration in the air, effectively smothering the fire, makes it a valuable component in fire suppression systems, particularly in sensitive environments such as data centers and server rooms.
Check Digit Verification of cas no
The CAS Registry Mumber 460-13-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 460-13:
(5*4)+(4*6)+(3*0)+(2*1)+(1*3)=49
49 % 10 = 9
So 460-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H7F/c1-2-3-4/h2-3H2,1H3
460-13-9Relevant academic research and scientific papers
Perfluorination of Allene Derivatives by Direct Fluorination
Arimura, Takashi,Shibakami, Motonari,Tamura, Masanori,Kurosawa, Shigeru,Sekiya, Akira
, p. 588 - 598 (2007/10/02)
Perfluoropropane was prepared from allene with elemental fluorine in the presence of sodium fluoride in 84percent yield for the first time.The reaction of allene with elemental fluorine afforded 2,2-difluoropropane in the absence of sodium fluoride.Methoxyallene and cyanoallene were perfluorinated with elemental fluorine in the presence of sodium fluoride to give heptafluoropropyl trifluoromethyl ether and heptafluoropropyl cyanide in good yields respectively.In addition, the direct fluorination of cyanoallene in the presence of cesium fluoride afforded N,N-difluorononafluorobutylamine in 95percent yield.
Fluorination of Alkanes by Chlorine Trifluoride. Hydride Abstraction Mechanism
Brower, K. R.
, p. 798 - 802 (2007/10/02)
Addition of chlorine trifluoride to a solution of alkane in Freon or liquid carbon dioxide at -75 deg C gives good yields of monofluoroalkane along with difluoro- and trifluoroalkanes in amounts dependent on reactant proportions.The inorganic products are HF and ClF.The reaction is highly selective for 3 over 2 positions.Methane and hexamethylethane are unreactive.Neohexane fluorinates with rearrangement, but 2-fluoro-3,3-dimethylbutane exposed to the postreaction medium does not rearrange.A hydride abstraction mechanism is inferred.
