382-30-9 Usage
Uses
Used in Organic Synthesis:
1,1,1-Trifluoro-2-(trifluoromethyl)-4-oxapentane is used as a solvent in organic synthesis for its ability to dissolve a wide range of compounds and facilitate chemical reactions. Its low reactivity and high stability contribute to its effectiveness in this application.
Used in Chemical Processes:
In the chemical industry, 1,1,1-Trifluoro-2-(trifluoromethyl)-4-oxapentane is used as a solvent in various chemical processes due to its inertness and ability to dissolve a broad spectrum of substances. This makes it a valuable component in the production of various chemicals and materials.
Used in Refrigeration Industry:
1,1,1-Trifluoro-2-(trifluoromethyl)-4-oxapentane is used as a refrigerant in the refrigeration industry. Its properties, such as low toxicity and high thermal stability, make it a suitable alternative to traditional refrigerants, contributing to more environmentally friendly cooling systems.
Used in Aerosol Products:
This fluorinated ether compound is also used as a propellant in aerosol products. Its low reactivity and ability to carry active ingredients make it an effective component in the formulation of various aerosol-based consumer and industrial products.
It is important to handle 1,1,1-Trifluoro-2-(trifluoromethyl)-4-oxapentane with care due to its potential health and environmental hazards. Proper safety measures should be taken to minimize risks associated with its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 382-30-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 382-30:
(5*3)+(4*8)+(3*2)+(2*3)+(1*0)=59
59 % 10 = 9
So 382-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H6F6O/c1-12-2-3(4(6,7)8)5(9,10)11/h3H,2H2,1H3
382-30-9Relevant academic research and scientific papers
Misaki, Susumu
, p. 471 - 475 (1985)
Methoxyperfluoroisobutene was converted to α-methylhexafluoroisobutyric acid fluoride by a catalytic amount of phase transfer catalyst in quantitative yield.
