6640-36-4 Usage
Chemical structure
A complex organic compound consisting of a naphthalene ring with a hydrazine group attached to it.
Classification
A hydrazone, a class of organic compounds often used in various chemical reactions.
Presence of phenyl group
The compound has a phenyl group on the hydrazine moiety, which makes it potentially useful in the synthesis of other organic molecules.
Potential applications
The structure of the compound suggests potential applications in the field of medicinal chemistry and organic synthesis.
Uses in chemical reactions
1-[(2-phenylhydrazino)methylidene]naphthalen-2(1H)-one may have potential uses in various chemical reactions.
Building block
The compound can be used as a building block for more complex compounds.
Molecular weight
Approximately 263.3 g/mol (calculated from the molecular formula)
Appearance
The compound is likely to be a solid, based on its molecular weight and complexity.
Stability
The stability of the compound may depend on factors such as temperature, pressure, and the presence of other chemicals. Further research would be needed to determine its stability under various conditions.
Solubility
The solubility of the compound is not provided in the material, but it can be inferred that it may be soluble in organic solvents such as ethanol, methanol, or acetone, due to its hydrazone nature.
Reactivity
The compound may be reactive with certain chemicals, such as acids, bases, or other nucleophiles, due to the presence of the hydrazine group and the phenyl group. Further research would be needed to determine its reactivity profile.
Check Digit Verification of cas no
The CAS Registry Mumber 6640-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6640-36:
(6*6)+(5*6)+(4*4)+(3*0)+(2*3)+(1*6)=94
94 % 10 = 4
So 6640-36-4 is a valid CAS Registry Number.
6640-36-4Relevant articles and documents
Facile synthesis of pyrazoles by iron-catalyzed regioselective cyclization of hydrazone and 1,2-diol under ligand-free conditions
Panda, Niranjan,Ojha, Subhadra
, p. 244 - 251 (2018/03/13)
A facile synthesis of pyrazoles by the cyclization of hydrazones and 1,2-diols was described. In the presence of ferric nitrate, the reaction occurs under neat conditions and makes the use of potassium persulfate to oxidize the diol to α-hydroxy carbaldehyde for the reaction with hydrazones to produce 1,3- and 1,3,5-substituted pyrazoles selectively. The overall regioselective transformation occurs in one-pot under ligand-free, mild conditions even in the presence of air.
