91165-74-1 Usage
Chemical structure
A complex compound with multiple functional groups, including a naphthalene ring, a triazole ring, and two carboxylic acid ester groups.
Ethoxycarbonyl group
Attached to the triazole ring, providing additional functionality and reactivity.
Research and pharmaceutical applications
Often used in the development of new drugs and organic synthesis processes due to its unique structure and functional groups.
Versatility
The compound's structure and functional groups make it suitable for a wide range of biological and chemical applications.
Naphthalene ring
A central part of the molecule, providing a planar, aromatic system that can interact with other molecules through π-π stacking or hydrophobic interactions.
Triazole ring
A five-membered ring containing three nitrogen atoms, which can participate in various chemical reactions and form hydrogen bonds.
Carboxylic acid ester groups
Two ester groups attached to the 4 and 5 positions of the triazole ring, which can undergo hydrolysis to form the corresponding carboxylic acids or react with other nucleophiles.
Esterification
The presence of ester groups indicates that the compound can be further modified through transesterification or other ester-based reactions.
Biological activity
The compound's unique structure and functional groups may contribute to its potential as a pharmacological agent or a building block for drug development.
Chemical synthesis
The compound can be used as a starting material or intermediate in the synthesis of more complex molecules, taking advantage of its reactive functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 91165-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,6 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91165-74:
(7*9)+(6*1)+(5*1)+(4*6)+(3*5)+(2*7)+(1*4)=131
131 % 10 = 1
So 91165-74-1 is a valid CAS Registry Number.
91165-74-1Relevant academic research and scientific papers
Synthesis and Spectroscopic Studies of 1,1'-(1,8-Naphthylene)di-1H-1,2,3-triazoles
Nagawa, Yoshinobu,Honda, Koichi,Nakanishi, Hiroshi
, p. 2931 - 2936 (2007/10/02)
The first 1,8-diheteroaromatic naphthalenes, 1,1'-(1,8-naphthylene)di-1H-1,2,3-trizoles (1), were synthesized by 1,3-dipolar cycloadditions of 1,8-diazidonaphthalene to acetylenic esters.The spectral properties of these compounds were studied and compared with those of the corresponding 1-(1-naphthyl)-1H-1,2,3-triazoles (2).The two triazole rings at the peri-positions in 1 are in a face-to-face arrangement according to the results of 1H NMR spectra.The UV spectra of 1 are almost identical with each other and show a red shift from those of corresponding 2.No significant spectral differences between 1 and 2 were observed in the IR spectra.The fragment ion with two azirine groups at the peri-position in the naphthalene ring was observed in the MS spectra of 1.
Syntheses and Spectroscopic Studies of 1,8-Bistriazolylnaphthalenes
Honda, Koichi,Nakanishi, Hiroshi,Nagawa, Yoshinobu,Yabe, Akira
, p. 450 - 451 (2007/10/02)
The first 1,8-diheterocyclic naphthalenes, the 1,8-bis(1'H-1',2',3'-triazolyl)naphthalenes (1a - i), have been synthesized by 1,3-dipolar cycloadditions of 1,8-diazidonaphthalene to acetylenic esters or enolates of acetoacetic esters, and have strained structures as revealed by comparison of their spectral properties with those of the corresponding 1-(1'H-1',2',3'-triazolyl)naphthalenes.
