559-92-2 Usage
Physical State
Colorless liquid at room temperature
The compound appears as a colorless liquid when not heated or pressurized.
Molecular Structure
Heptafluoro-1-(4-methylphenyl)group attached to a butanone backbone
The presence of seven fluorine atoms and a methylphenyl group provides unique chemical properties and stability.
Industrial Uses
Solvent in the production of plastics, paints, and adhesives
Due to its unique properties, the compound is commonly used as a solvent in various industrial processes.
Chemical Synthesis
Reagent in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals
The compound is utilized as a reagent in the synthesis of various organic compounds, including pharmaceuticals and specialty chemicals.
Stability
Increased stability due to the presence of fluorine and methylphenyl groups
The heptafluoro-1-(4-methylphenyl)group enhances the stability of the 1-butanone molecule, making it suitable for a wide range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 559-92-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 559-92:
(5*5)+(4*5)+(3*9)+(2*9)+(1*2)=92
92 % 10 = 2
So 559-92-2 is a valid CAS Registry Number.
559-92-2Relevant academic research and scientific papers
HALOGENATED OXIME DERIVATIVES AND THE USE THEREOF AS LATENT ACIDS
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Page 65, (2008/06/13)
Compounds of the formula (I) or (II) wherein R1 is C1-C10haloalkylsulfonyl, halobenzenesulfonyl, C2-C10haloalkanoyl, halobenzoyl; R2 is halogen or C1-C10haloalkyl; Arl is phenyl, biphenylyl, fluorenyl, naphthyl, anthracyl, phenanthryl, or heteroaryl, all
