3362-58-1 Usage
Chemical structure
A derivative of cycloheptatriene with an amine group, a phenylmethyl group attached to the amine nitrogen, and an imino group attached to the cycloheptatrienamine.
Functional groups
Contains an amine group (-NH2), a phenylmethyl group (-C6H5CH2-), and an imino group (=N-).
Potential applications
Organic synthesis and pharmaceutical research due to its unique structure and functional groups.
Importance for research
Understanding the properties and reactivity of 1,3,5-Cycloheptatrien-1-amine,N-(phenylmethyl)- 7-[(phenylmethyl)imino]- is crucial for determining its potential uses and applications in various industries.
Reactivity
The presence of multiple functional groups may lead to various chemical reactions, such as nucleophilic substitution, electrophilic aromatic substitution, and imine formation.
Structural features
The cycloheptatriene core provides a seven-membered ring, which may influence the compound's stability and reactivity.
Molecular weight
Approximately 349.49 g/mol (calculated from the molecular formula).
Stereochemistry
The compound may exhibit stereoisomerism due to the presence of a phenylmethyl group and the cycloheptatrienamine core.
Solubility
The compound's solubility profile is not provided, but it may be influenced by the presence of the amine, phenylmethyl, and imino groups.
Stability
The stability of the compound may be affected by the presence of the amine and imino groups, which can participate in various reactions.
Synthesis
The synthesis of 1,3,5-Cycloheptatrien-1-amine,N-(phenylmethyl)- 7-[(phenylmethyl)imino]- may involve the formation of the cycloheptatriene core, followed by the introduction of the amine, phenylmethyl, and imino groups through appropriate chemical reactions.
Analytical techniques
Techniques such as NMR, IR, and mass spectrometry can be used to analyze and confirm the structure of 1,3,5-Cycloheptatrien-1-amine,N-(phenylmethyl)- 7-[(phenylmethyl)imino]- .
Hazards and safety
The compound's hazards and safety profile are not provided, but it should be handled with care due to the presence of reactive functional groups. Appropriate safety measures should be taken during synthesis and handling.
Check Digit Verification of cas no
The CAS Registry Mumber 3362-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3362-58:
(6*3)+(5*3)+(4*6)+(3*2)+(2*5)+(1*8)=81
81 % 10 = 1
So 3362-58-1 is a valid CAS Registry Number.
3362-58-1Relevant academic research and scientific papers
Novel fluorophores: Syntheses and photophysical studies of boron-aminotroponimines
Balachandra, Chenikkayala,Sharma, Nagendra K.
, p. 532 - 538 (2016/12/09)
The syntheses and photophysical study of novel fluorescent boron-aminotroponimine complexes are described. The chemical structure of one of the boron complexes was confirmed by single crystal X-ray analysis, which shows the appearance of the distorted tetrahedral geometry at boron. The photophysical studies of these complexes revealed that the boron-aminotroponimines are fluorescent molecules with quantum yields ca. 0.17–0.28.
Intramolecular hydroamination with homogeneous zinc catalysts: Evaluation of substituent effects in N,N′-disubstituted aminotroponiminate zinc complexes
Dochnahl, Maximilian,Loehnwitz, Karolin,Pissarek, Jens-Wolfgang,Biyikal, Mustafa,Schulz, Sabrina R.,Schoen, Sebastian,Meyer, Nils,Roesky, Peter W.,Blechert, Siegfried
, p. 6654 - 6666 (2008/03/14)
A series of symmetrical and unsymmetrical N,N′-disubstituted aminotroponimines (ATIHs) have been prepared. Substituents ranging from linear to cyclic alkyl groups, chelating ethers, and aryl groups were employed. The corresponding aminotroponiminate zinc
Acylotropic tautomerism: XXXV. R?L-inversion of configuration of dipolar spyrocyclic and open-chain 2-arylaminotropone isomers
Olekhnovich,Budarina,Borodkin,Kurbatov,Vaslyaeva,Zhdanov
, p. 713 - 722 (2007/10/03)
R?L-Inversion of chiral spirocyclic and open-chain 2-arylaminotropone derivatives with varied heteroatom (O, S, N) has been studied. Kinetic relations holding in the R,L-permutation are discussed. Its mechanism includes formation and dissociation of spiro bonds and torsion stereodynamics.
Synthesis of 2-Aminotropone Oximes and 2-Alkoxytropone Imines
Nozoe, Tetsuo,Lin, Lung Ching,Hsu, Chih-Hsien,Tsay, Shwu-Chen,Hakimelahi, Gholam H.,Hwu, Jih Ru
, p. 362 - 363 (2007/10/03)
A synthetic route was developed for preparation of 2-aminotropone oximes 10-14, a new class of compounds, from tropolone 2; 2-methoxytropone imines 7-9 and tropylium salts 17 were generated as the key intermediates.
A Facile Synthesis of N,N'-Dialkyl-2-aminotroponimines
Mimata, Yuzo,Saisho, Tomoko,Hamada, Masaharu,Imafuku, Kimiaki
, p. 156 (2007/10/03)
Seven N,N'-dialkyl-2-aminotroponimines (alkyl = Me, Et, Prn, Pri, Bun, Bui or CH2Ph) are prepared by the reaction of benzocycloheptoxazine with the alkylamine.
