7477-68-1 Usage
Molecular Weight
329.44 g/mol
Structure
A derivative of prop-2-en-1-one (Acetophenone) with a piperidine group and multiple phenyl groups attached.
Functional Groups
Carbonyl group (C=O) in the prop-2-en-1-one core
Aromatic rings (Phenyl groups) attached to the core
A cyclic amine (Piperidine group) attached to the core
Appearance
Likely a solid or oily liquid, depending on the conditions
Solubility
Soluble in organic solvents like ethanol, methanol, and dichloromethane
Stability
Stable under normal conditions, but sensitive to heat, light, and moisture
Reactivity
Can undergo reactions typical of carbonyl compounds, such as nucleophilic addition, reduction, and condensation reactions
Biological Activity
Potential biological activity, depending on the specific application and context
Applications
Commonly used in pharmaceutical research and organic synthesis due to its unique structure
Hazards
Potential irritant or toxic, depending on the dose and exposure route; proper handling and safety precautions are necessary
Storage
Should be stored in a cool, dry, and well-ventilated area, away from heat and light sources, and in a sealed container to prevent degradation or contamination.
Check Digit Verification of cas no
The CAS Registry Mumber 7477-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7477-68:
(6*7)+(5*4)+(4*7)+(3*7)+(2*6)+(1*8)=131
131 % 10 = 1
So 7477-68-1 is a valid CAS Registry Number.
7477-68-1Relevant articles and documents
Dual mechanism of enamine-enamine rearrangement of 1,3-diaryl-3-(1-imidazolyl)propen-2-ones
Rekhter,Rekhter
, p. 593 - 594 (2002)
The formation of 1,3-diaryl-3-(1-imidazolyl)propen-1,3-diol that is an intermediate of enamine-enamine rearrangement of 1,3-diaryl-3-(1-imidazolyl)propen-1-ones constitutes the key stage of the dual mechanism of the rearrangement proper. The reaction of 1,3-diaryl-2,3-dibromopropan-1-ones with a primary amine provides 1,3-diaryl-3-iminopropan-1-ones as a result of enamine-imine prototropic rearrangement.
TRISUBSTITUTED THIAZOLES BY A 6?-ELECTROCYCLIZATION OF IMINOTHIOCARBONYL YLIDES
Corsaro, A.,Tarantello, M.,Purrello, G.
, p. 3305 - 3308 (2007/10/02)
Iminothiocarbonyl ylides are generated by a sulfur ligand exchange reaction of sulfonium salts and undergo a 6?-electrocyclic closure and aromatization to tri substituted thiazoles.Related carbonyl ylides preferred a 4?-electrocyclization.
