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1,4,7,10,13-Pentaoxa-16-azacyclooctadecane, 16-[(3,3-diphenyl-3H-naphtho[2,1-b]pyran-5-yl)methyl]- is a crowned chromene derivative featuring an aza-18-crown-6 ether moiety linked to a naphthopyran core. 1,4,7,10,13-Pentaoxa-16-azacyclooctadecane, 16-[(3,3-diphenyl-3H-naphtho[2,1-b]pyran-5-yl)methyl]- exhibits enhanced photochromic properties in the presence of metal ions due to the strong interaction between the crown ether and the bound cation, leading to significant red-shifts in absorption spectra and accelerated thermal and photoisomerization kinetics compared to non-crowned analogs. The aza-18-crown-6 unit selectively complexes alkali, alkaline earth, and transition metal ions, influencing the photochromic behavior of the naphthopyran system. Other names for 1,4,7,10,13-Pentaoxa-16-azacyclooctadecane, 16-[(3,3-diphenyl-3H-naphtho[2,1-b]pyran-5-yl)methyl]- may include: - Crowned naphthopyran-aza-18-crown-6 ether conjugate - 16-[(3,3-Diphenyl-3H-naphtho[2,1-b]pyran-5-yl)methyl]-1,4,7,10,13-pentaoxa-16-azacyclooctadecane - Aza-18-crown-6-functionalized naphthopyran.

579510-35-3

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579510-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 579510-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,9,5,1 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 579510-35:
(8*5)+(7*7)+(6*9)+(5*5)+(4*1)+(3*0)+(2*3)+(1*5)=183
183 % 10 = 3
So 579510-35-3 is a valid CAS Registry Number.

579510-35-3Downstream Products

579510-35-3Relevant academic research and scientific papers

Investigation of cation complexation behavior of azacrown ether substituted benzochromene

Fedorova,Maurel,Chebun'kova,Strokach,Valova,Kuzmina,Howard,Wenzel,Gloe,Lokshin,Samat

, p. 469 - 483 (2007)

The study of the complex formation of 3,3-diphenyl-3H-benzo[f]chromenes containing aza-18-crown-6-ether, diaza-18-crown-6-ether or morpholine units with alkali, alkaline earth, heavy and transition metal cations in acetonitrile is reported. The spectrosco

Synthesis and photochromism of novel chromene derivatives bearing a monoazacrown ether moiety

Ahmed, Saleh A.,Tanaka, Mutsuo,Ando, Hisanori,Iwamoto, Hitoshi,Kimura, Keiichi

, p. 2437 - 2442 (2003)

Crowned chromenes - four novel naphthopyrans (chromenes) bearing monoaza-12-crown-4, -15-crown-5, -18-crown-6, and a noncyclic analogue at the 5-position-were synthesized, and their photochromism in acetonitrile was examined in the presence of alkali and alkaline-earth metal ions. Incorporation of crown ether units to chromene moieties facilitated to a great extent both the thermal isomerization and photoisomerization of the chromene moiety, reflecting the metal-ion-binding ability of the crown ether moiety. Comparison of the crowned chromenes with the corresponding crowned spirobenzopyrans reveals that photochromism of the crowned chromene reflects an interaction between the metal ion and the crown ether moiety that is stronger than that of the crowned spirobenzopyran, and shows only positive photochromism with significant red-shifts in the UV/Vis absorption spectra, in contrast to the crowned spirobenzopyrans reported previously. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).

Investigation of the azacrown-ether substituted naphtopyranes

Chebun'kova,Gromov,Strokach, Yu P.,Valova,Alfimov,Fedorova,Lokshin,Samat

, p. 67 - 73 (2005)

The study of the complexation of 3,3-diphenyl-3H-benzo[f]chromenes containing an aza-15-crown-5-ether or morpholine units with Mg2+, Ba2+ and Pb2+ in acetonitrile are reported. The spectroscopic and kinetic behaviour of th

Synthesis and complexation properties of photochromic benzochromenes containing aza- and diaza- 18-crown-6-ether fragments

Fedorova,Strokach,Chebun'kova,Valova,Gromov,Alfimov,Lokshin,Samat

, p. 287 - 294 (2007/10/03)

Complex formation of Mg2+, Ba2+, and Pb2+ perchlorates with 3,3-diphenyl-3H-benzo[f]chromenes containing aza-and diaza-18-crown-6-ether or morpholine fragments was studied. The strong influence of the metal cations on the

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