368-35-4 Usage
Uses
Used in the Food Industry:
BUTYL 2,2-DIFLUOROACETATE is used as a flavoring agent for its pleasant fruity odor, enhancing the taste and aroma of various food products.
Used in the Perfume Industry:
BUTYL 2,2-DIFLUOROACETATE is used as a scent ingredient in the production of perfumes, contributing to the creation of unique and appealing fragrances.
Used in Pharmaceutical Production:
BUTYL 2,2-DIFLUOROACETATE serves as an intermediate in the synthesis of pharmaceuticals, playing a crucial role in the development of various medications.
Used in Organic Synthesis:
As a solvent or intermediate, BUTYL 2,2-DIFLUOROACETATE is utilized in organic synthesis for the production of a wide range of chemical compounds and materials.
Used in Industrial Applications:
BUTYL 2,2-DIFLUOROACETATE is employed in several industrial applications due to its versatility and low toxicity, making it a relatively safe option for diverse uses.
Check Digit Verification of cas no
The CAS Registry Mumber 368-35-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 368-35:
(5*3)+(4*6)+(3*8)+(2*3)+(1*5)=74
74 % 10 = 4
So 368-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15F5O2/c1-3-8(17)7(9(18)4-2)5-6-10(12,13)11(14,15)16/h7H,3-6H2,1-2H3
368-35-4Relevant academic research and scientific papers
Lithium sulfur battery
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, (2012/09/05)
A lithium sulfur battery comprising an electrolyte solvent which comprises at least one fluorosubstituted compound is described. Preferred fluorosubstituted compounds which are predominantly solvents are notably selected from the group consisting of fluorosubstituted carboxylic acid esters, fluorosubstituted carboxylic acid amides, fluorosubstituted fluorinated ethers, fluorosubstituted carbamates, fluorosubstituted cyclic carbonates, fluorosubstituted acyclic carbonates, fluorosubstituted ethers, perfluoroalkyl phosphoranes, fluorosubstituted phosphites, fluorosubstituted phosphates, fluorosubstituted phosphonates, and fluorosubstituted heterocycles. Monofluoroethylene carbonate, cis-difluoroethylene carbonate, trans-difluoroethylene carbonate, 4,4-difluoroethylene carbonate, trifluoroethylene carbonate, tetrafluoroethylene carbonate, 4-fluoro-4-methyl-1,3-dioxolane-2-one, 4-fluoro-4-ethyl-1,3-dioxolane-2-one, 2,2,2-trifluoroethyl-methyl carbonate, 2,2,2-trifluoroethyl-fluoromethyl carbonate are preferred. The solvent may further comprise a non-fluorinated solvent, e.g., ethylene carbonate, a dialkyl carbonate, or propylene carbonate. Use of such fluorinated compound as additive for such batteries and specific electrolyte solutions.
