86864-47-3 Usage
Chemical class
Aryl-phenylketones
Structure
Central butan-1-ol chain with a tritylsulfanyl group attached to the third carbon atom and a phenylimino group attached to the first carbon atom
Functionality
Synthetic intermediate in the production of various organic compounds and pharmaceuticals
Use
Building block in organic synthesis and as a reagent in chemical reactions
Biological and pharmacological activities
Studied for potential applications, but further research is needed
Solubility
Likely soluble in organic solvents such as ethanol, methanol, or dichloromethane
Stability
Stable under normal laboratory conditions, but sensitive to heat, light, and moisture
Reactivity
May react with strong acids, strong bases, or nucleophiles
Purity
Typically synthesized with high purity, but may contain trace amounts of impurities or side products
Safety
Handle with care, as it may have unknown toxicological properties or hazards
Storage
Store in a cool, dry, and well-ventilated area, away from heat, light, and moisture
Disposal
Dispose of according to local regulations and guidelines for chemical waste
Appearance
May appear as a colorless to pale yellow solid or oil, depending on the purity and synthesis method
Melting point
Varies depending on the specific synthesis and purity, but generally has a melting point in the range of 100-150°C
Boiling point
Not well-defined due to the compound's complex structure, but likely has a high boiling point due to its molecular weight and complexity
Check Digit Verification of cas no
The CAS Registry Mumber 86864-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,6 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86864-47:
(7*8)+(6*6)+(5*8)+(4*6)+(3*4)+(2*4)+(1*7)=183
183 % 10 = 3
So 86864-47-3 is a valid CAS Registry Number.
86864-47-3Relevant academic research and scientific papers
Studies on the Preparation and Reactions of Tritylsulfenimines
Branchaud, Bruce P.
, p. 3531 - 3538 (2007/10/02)
Carbonyl compounds react with stable, crystalline triphenylmethanesulfenamide (TrSNH2, 4) under mild conditions to form tritylsulfenimines 5 and 6.Lithiation of acetone tritylsulfenimine (5c) at O deg C led to a novel rearrangement-decomposition producing
