65352-91-2 Usage
Chemical classification
Epiminodibenzo[b,f][1,5]dioxocine, a type of organic compound.
Molecular structure
Complex and specific, with a methyl group at the 13th position.
Functional groups
Contains a dibenzo[b,f][1,5]dioxocine core and an epoxide group.
Position of methyl group
13th position in the molecule.
Potential applications
Possible uses in pharmaceuticals, research, and other industries.
Further study
Additional research may be needed to fully understand its properties and potential uses.
Molecular weight
Approximately 240.26 g/mol (calculated from the chemical formula).
Stereochemistry
The presence of an epoxide group may introduce stereochemistry to the molecule.
Solubility
Solvent compatibility may vary depending on the specific functional groups and molecular structure.
Stability
The stability of the compound may depend on factors such as temperature, light exposure, and the presence of other reactive substances.
Toxicity
The toxicity of the compound is not mentioned in the provided material, but it should be considered when evaluating potential applications.
Environmental impact
The environmental impact of the compound is not mentioned in the provided material, but it should be considered when evaluating potential applications.
Synthesis
The synthesis of the compound may involve multiple steps and the use of various reagents, depending on the specific molecular structure.
Check Digit Verification of cas no
The CAS Registry Mumber 65352-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65352-91:
(7*6)+(6*5)+(5*3)+(4*5)+(3*2)+(2*9)+(1*1)=132
132 % 10 = 2
So 65352-91-2 is a valid CAS Registry Number.
65352-91-2Relevant articles and documents
Proton transfer reaction in N-methyl-2-hydroxy-schiff bases aleksander filarowski 1,3
Koll, Aleksander,Glowiak, Tadeusz,Majewski, Eugeniusz,Dziembowska, Teresa
, p. 393 - 402 (2007/10/03)
The structure of two ortho-hydroxy N-methyl Schiff hases as well as the selfcondensation product of 2-(N-methyHminome:hyl)-phenol are determined by X-Ray crystallography and by ab initio DFT, on B3LYP/631G** level, calculations. Electronic coupling between acidic and basic centres of the molecules, especially effective in the proton transfer structure, is discussed on the basis of detailed analysis of differentiation of bond lengths both in aromatic and chelate rings. Consequences of this coupling or, the intramolecular hydrogen bonding and proton transfer process are discussed. WILEY-VCH Verlag GmbH 1998.
