21379-33-9 Usage
Uses
Used in Chemical Industry:
1,3-Butanediol, 4,4,4-trifluoro-3-(trifluoromethyl)is used as a solvent for the production of resins, coatings, and adhesives due to its high solvency and low toxicity, which contribute to the efficiency and quality of these products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,3-Butanediol, 4,4,4-trifluoro-3-(trifluoromethyl)is utilized as a solvent in the synthesis of various pharmaceuticals, leveraging its chemical properties to facilitate the production of medications with improved efficacy and safety profiles.
Used in Agricultural Chemical Industry:
1,3-Butanediol, 4,4,4-trifluoro-3-(trifluoromethyl)is also employed as a solvent in the synthesis of agricultural chemicals, where its properties aid in the creation of more effective and safer agrochemicals for crop protection and enhancement.
These applications highlight the importance of 1,3-Butanediol, 4,4,4-trifluoro-3-(trifluoromethyl)as a key component in a wide range of industrial processes, underpinning its value in enhancing the performance and safety of final products.
Check Digit Verification of cas no
The CAS Registry Mumber 21379-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,7 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21379-33:
(7*2)+(6*1)+(5*3)+(4*7)+(3*9)+(2*3)+(1*3)=99
99 % 10 = 9
So 21379-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H6F6O2/c6-4(7,8)3(13,1-2-12)5(9,10)11/h12-13H,1-2H2
21379-33-9Relevant academic research and scientific papers
Methods for Producing Fluorine-Containing Hydroxyaldehyde, Fluorine-Containing Propanediol, and Fluorine-Containing Alcohol Monomer
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Paragraph 0221, (2015/12/30)
As shown by the following reaction formula, disclosed is a fluorine-containing hydroxyaldehyde production method, including the step of obtaining a fluorine-containing hydroxyaldehyde represented by the general formula (1) by reacting a fluorine-containin
PROCESS FOR PREPARING FLUORINATED DIOLS
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Page/Page column 7, (2012/09/10)
A process for preparing a fluorinated diol compound by reacting the corresponding ketone-alcohol or aldehyde-alcohol with hydrogen over a palladium catalyst in the vapor phase.
THE REACTION OF SOME 3- AND 4-FLUOROOXETANES WITH ACIDS
Tarrant, Paul,Bull, R. N.
, p. 201 - 216 (2007/10/02)
Several oxetanes prepared from hexafluoroacetone and hydrofluoroolefins were treated with aluminum chloride.Substitution of fluorine by chlorine occured on the 3- and 4-carbon atoms as well as cleavage of the ether leakage to give chloroalkyl carbinols or in, some cases, vinyl carbinols.Individual samples of the cis and trans-3,4-difluorooxetanes formed roughly equivalent amounts of the 3-fluoro-4-chlorooxetane stereoisomers, indicating a common carbonium intermediate.Treatment of the 4-fluorooxetane with sulfuric acid gave a dioxetane, a dioxene and an unsaturated aldehyde.
