240417-93-0 Usage
Molecular structure
A phenol group attached to a 1,4-diazepine ring with a trifluoromethyl group at the 7 position.
Derivative of diazepine
The compound is derived from a seven-membered heterocyclic compound containing two nitrogen atoms in the ring.
Trifluoromethyl group
A functional group known for its electron-withdrawing properties, which can influence the reactivity and stability of the compound.
Phenol group
A hydroxyl group attached to a benzene ring, making the compound potentially reactive in various chemical reactions.
Potential applications
May have applications in pharmaceutical research or as a building block in organic synthesis.
Reactivity
The compound's potential to participate in chemical reactions due to the presence of the phenol and trifluoromethyl groups.
Stability
The compound's ability to maintain its structure and properties under various conditions, which would depend on its chemical characteristics.
Chemical characteristics
Specific properties of the compound, such as solubility, boiling point, and melting point, which would influence its potential uses and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 240417-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,4,1 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 240417-93:
(8*2)+(7*4)+(6*0)+(5*4)+(4*1)+(3*7)+(2*9)+(1*3)=110
110 % 10 = 0
So 240417-93-0 is a valid CAS Registry Number.
240417-93-0Relevant articles and documents
Reactions of aromatic and heteroaromatic β-amino-β-polyfluoroalkylvinyl ketones with ethylenediamine. A new synthesis of N,N′-unsubstituted imidazolidines
Sosnovskikh,Kutsenko
, p. 540 - 551 (2007/10/03)
The reactions of aromatic and heteroaromatic β-amino-β-polyfluoroalkylvinyl ketones with ethylenediamine results in the formation of 2,3-dihydro-1H-1,4-diazepines, N,N′-unsubstituted imidazolidines, or N,N′-ethylenebis(aminovinyl ketones). The reaction route depends on the reaction conditions, the nature of the substituent at the carbonyl group, and the number of fluorine atoms in the polyfluoroalkyl radical.
Reactions of 2-polyfluoroalkylchromones with aliphatic diamines
Sosnovskikh,Kutsenko
, p. 812 - 814 (2007/10/03)
2-Polyfluoroalkylchromones react with aliphatic 1,2-diamines to give 2,3-dihydro-1H-1,4-diazepines. A similar reaction with 1,3-diaminopropane yields N,N′-trimethylenebis(2-hydroxyacetophenonimines) as a result of scission of the original chromones.
