Tag: 411.5387

Favaro, Gianna et al. published their research in Molecular Crystals and Liquid Crystals Science and Technology in 1994 | CAS: 114747-45-4

1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Some chemotherapeutic agents have piperidine moiety within their structure, foremost among them, vinblastine and raloxifene.Safety of 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine]

Triplet reactivity of spiroindolinooxazines studied by photosensitization was written by Favaro, Gianna;Malatesta, Vincenzo;Mazzucato, Ugo;Ottavi, Gaetano;Romani, Aldo. And the article was included in Molecular Crystals and Liquid Crystals Science and Technology in 1994.Safety of 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] This article mentions the following:

The quantum yields for the direct and triplet sensitized color-forming reactions of five spiroindolinooxazines were determined in methylcyclohexane. Higher triplet than singlet reactivities were generally found. In the experiment, the researchers used many compounds, for example, 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4Safety of 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine]).

1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Some chemotherapeutic agents have piperidine moiety within their structure, foremost among them, vinblastine and raloxifene.Safety of 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine]

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

 

Luchina, V. G. et al. published their research in Journal of Photochemistry and Photobiology, A: Chemistry in 1996 | CAS: 114747-45-4

1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4) belongs to piperidine derivatives. Piperidine is a saturated organic heteromonocyclic parent, an azacycloalkane, a secondary amine and a member of piperidines. Fluorinated piperidines are also the subject of continued interest in medicinal chemistry, for example in the synthesis of selective dipeptidyl peptidase II (DPP II) inhibitors. Piperidine derivatives are also used in solid-phase peptide synthesis (SPPS) and many degradation reactions.Related Products of 114747-45-4

Photochromism of spironaphthooxazines having electron-donor substituents was written by Luchina, V. G.;Sychev, I. Yu.;Shienok, A. I.;Zaichenko, N. L.;Marevtsev, V. S.. And the article was included in Journal of Photochemistry and Photobiology, A: Chemistry in 1996.Related Products of 114747-45-4 This article mentions the following:

Spectral and photochromic properties of spironaphthooxazines (SNOs) with piperidine and morpholine substituents have been studied at different temperatures in various solvents. It has been recognized that introduction of these substituents in naphthooxazine fragment leads to fluorescence of the initial form of SNO mols. at low temperatures, which disappears with temperature rise. The dependences of the photoinduced form of spectral characteristics on temperature and concentration make it possible to assume the aggregation of the mols. of photoinduced form in non-polar solvents. It is proposed that the colored form of substituted SNOs has a bipolar structure with a pos. charge on piperidine or morpholine nitrogen atom contrary to the quinonoic form of unsubstituted SNO. In the experiment, the researchers used many compounds, for example, 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4Related Products of 114747-45-4).

1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4) belongs to piperidine derivatives. Piperidine is a saturated organic heteromonocyclic parent, an azacycloalkane, a secondary amine and a member of piperidines. Fluorinated piperidines are also the subject of continued interest in medicinal chemistry, for example in the synthesis of selective dipeptidyl peptidase II (DPP II) inhibitors. Piperidine derivatives are also used in solid-phase peptide synthesis (SPPS) and many degradation reactions.Related Products of 114747-45-4

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

 

De Filpo, Giovanni et al. published their research in Liquid Crystals in 2017 | CAS: 114747-45-4

1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4) belongs to piperidine derivatives. The piperidine moiety constitutes an important building block for the synthesis of a variety of bioactive natural products, alkaloids and other drugs. Piperidine prefers a chair conformation, similar to cyclohexane. Unlike cyclohexane, piperidine has two distinguishable chair conformations: one with the N–H bond in an axial position, and the other in an equatorial position.Formula: C27H29N3O

Preparation and characterization of bifunctional reverse-mode polymer-dispersed liquid crystals was written by De Filpo, Giovanni;Formoso, Patrizia;Manfredi, Sabrina;Mashin, Alexander I.;Nicoletta, Fiore P.. And the article was included in Liquid Crystals in 2017.Formula: C27H29N3O This article mentions the following:

Reverse-mode polymer-dispersed liquid crystals (PDLCs) are transparent films in their OFF state (no applied elec. field) and become opaque in their ON state. The addition of a photo-chromic compound allows a color change of films, when they are UV-irradiated. The aim of this work was the preparation and characterization of bifunctional materials, able to change their transparency by application of an elec. field and color under UV irradiation In particular, the performance of reverse-mode PDLCs doped with different spiro(indolo)-oxazine mols. was investigated. Both the electro-optical and photo-chromic response of these systems were evaluated and compared. In the experiment, the researchers used many compounds, for example, 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4Formula: C27H29N3O).

1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4) belongs to piperidine derivatives. The piperidine moiety constitutes an important building block for the synthesis of a variety of bioactive natural products, alkaloids and other drugs. Piperidine prefers a chair conformation, similar to cyclohexane. Unlike cyclohexane, piperidine has two distinguishable chair conformations: one with the N–H bond in an axial position, and the other in an equatorial position.Formula: C27H29N3O

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

 

Favaro, Gianna et al. published their research in Molecular Crystals and Liquid Crystals Science and Technology in 1994 | CAS: 114747-45-4

1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Some chemotherapeutic agents have piperidine moiety within their structure, foremost among them, vinblastine and raloxifene.Safety of 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine]

Triplet reactivity of spiroindolinooxazines studied by photosensitization was written by Favaro, Gianna;Malatesta, Vincenzo;Mazzucato, Ugo;Ottavi, Gaetano;Romani, Aldo. And the article was included in Molecular Crystals and Liquid Crystals Science and Technology in 1994.Safety of 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] This article mentions the following:

The quantum yields for the direct and triplet sensitized color-forming reactions of five spiroindolinooxazines were determined in methylcyclohexane. Higher triplet than singlet reactivities were generally found. In the experiment, the researchers used many compounds, for example, 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4Safety of 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine]).

1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine] (cas: 114747-45-4) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Some chemotherapeutic agents have piperidine moiety within their structure, foremost among them, vinblastine and raloxifene.Safety of 1,3,3-Trimethyl-6′-(piperidin-1-yl)spiro[indoline-2,3′-naphtho[2,1-b][1,4]oxazine]

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem