38253-21-3 Usage
Class
Organic compound, belonging to the class of cyclohexanones
Substituent
Ethyl(phenyl)amino group attached at the 2-position of cyclohexanone
Usage
Commonly employed as a reactant in organic synthesis
Utilized in pharmaceutical research
Potential Applications
Explored for medicinal purposes
Investigated for applications in material science
Properties
Physical State: Typically a solid at room temperature
Odor: May have a characteristic odor depending on purity and handling conditions
Solubility: Soluble in certain organic solvents, such as ethanol and acetone
Melting Point: Specific value may vary, but generally falls within a certain range
Boiling Point: Varies depending on purity and atmospheric pressure
Reactivity
Reacts with various reagents in organic synthesis reactions
May undergo functional group transformations under specific conditions
Toxicity
Toxicity profile may vary; precautions should be taken during handling and synthesis
Stability
Stability under different environmental conditions should be considered during storage and usage
Analytical Methods
Analyzed using techniques such as chromatography and spectroscopy for identification and quantification
References
Relevant literature and research papers on its synthesis, properties, and applications
Check Digit Verification of cas no
The CAS Registry Mumber 38253-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,5 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38253-21:
(7*3)+(6*8)+(5*2)+(4*5)+(3*3)+(2*2)+(1*1)=113
113 % 10 = 3
So 38253-21-3 is a valid CAS Registry Number.
38253-21-3Relevant articles and documents
Light-induced Reactions of 2-(N-Alkyl-N-arylamino)cyclohexanones and Related Amino-cycloalkanones: Formation of 7-Azabicyclooctan-1-ols
El-Hamamy, Ahmad A.,Hill, John,Townend, John
, p. 573 - 580 (2007/10/02)
On irradiation, 2-(N-alkyl-N-arylamino)cyclohexanones (aryl = Ph; alkyl = Me, benzyl, allyl, Et, CH2CH2Ph, or CH2CF3; or aryl = p-tolyl; alkyl = Me) (10) or (20), 4,4-dimethyl-2-(N-methylanilino)-cyclohexanone (24), and 2-(N-methylanilino)-5α-cholestan-3-one (26) underwent type-II cyclisation to afford azetidinol (7-azabicyclooctan-1-ol) derivatives.In general, fission to give the corresponding N-alkyl-N-arylamine and ketone was a minor photoreaction.When the alkyl group of the 2-(N-alkylanilino)cyclohexanone had the structure -CH(R)CH2R', a double 1,5-hydrogen transfer occurred leading to a low yield of a 2-anilinocyclohexanol (31a).Photolysis of 2-anilinocyclohexanone (32a) gave a little of the direct-fission product aniline (17a), and the alkylamino-ketones 2-(NN-diethylamino)- (32b) and 2-(N-pyrrolidino)-cyclohexanone (32c) underwent no significant photoreaction in methanol.The isolation of indan-1-one and N-trideuteriomethylaniline on irradiation of 2-(N-trideuteriomethylanilino)-indan-1-one (33b) in diethyl ether indicated that the photoreaction was a direct Cα-N bond fission and not a type-II fission.
