667870-42-0 Usage
Description
(7aR,11R,13S)-11-(1H-benzotriazol-1-yl)-7a,8,10,11-tetrahydro-13-phenyl-9H,13H-naphtho[1,2-e]pyrido[2,1-b][1,3]oxazine is a complex organic molecule that belongs to the class of naphthopyrido oxazine derivatives. It features a unique structure with a benzotriazole moiety and a phenyl group attached to a naphtho-pyrido-oxazine core, which may contribute to its potential applications in various fields.
Uses
Used in Pharmaceutical Applications:
(7aR,11R,13S)-11-(1H-benzotriazol-1-yl)-7a,8,10,11-tetrahydro-13-phenyl-9H,13H-naphtho[1,2-e]pyrido[2,1-b][1,3]oxazine is used as a potential pharmaceutical compound for its diverse structural features and possible biological activities. Its unique structure may allow it to interact with various biological targets, making it a candidate for the development of new drugs.
Used in Materials Science:
In the field of materials science, (7aR,11R,13S)-11-(1H-benzotriazol-1-yl)-7a,8,10,11-tetrahydro-13-phenyl-9H,13H-naphtho[2-e]pyrido[2,1-b][1,3]oxazine may be utilized for the development of novel materials with specific properties. Its structural characteristics could be exploited to create materials with applications in areas such as electronics, optics, or advanced coatings.
Used in Chemical Research:
(7aR,11R,13S)-11-(1H-benzotriazol-1-yl)-7a,8,10,11-tetrahydro-13-phenyl-9H,13H-naphtho[2-e]pyrido[2,1-b][1,3]oxazine is also used as a subject of chemical research to better understand its synthesis, characterization, and properties. This knowledge could lead to the discovery of new applications and the development of related compounds with improved or novel functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 667870-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,7,8,7 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 667870-42:
(8*6)+(7*6)+(6*7)+(5*8)+(4*7)+(3*0)+(2*4)+(1*2)=210
210 % 10 = 0
So 667870-42-0 is a valid CAS Registry Number.
667870-42-0Relevant articles and documents
Enantiopure 2,6-disubstituted piperidines bearing one alkene- or alkyne-containing substituent: Preparation and application to total syntheses of indolizidine-alkaloids
Liu, Hui,Su, Deyong,Cheng, Guolin,Xu, Jimin,Wang, Xinyan,Hu, Yuefei
scheme or table, p. 1899 - 1904 (2010/08/21)
A general and efficient procedure for the preparation of 2,6-disubstituted piperidines bearing one alkene- or alkyne-containing substituent was developed by using non-racemic Betti base as a chiral auxiliary. Many chiral benzylamines are excellent auxiliaries, but they were rarely used for this purpose because of the inefficient removal of the N-benzyl auxiliary residue under non-hydrogenative conditions. We found that N,N-disubstituted Betti base derivative has a typical Mannich structure of o-naphthol. When it carried out a base-catalyzed formation of o-quinone methide, an efficient non-hydrogenative N-debenzylation was achieved, and the alkene and alkyne groups survived. To demonstrate the efficiency of the method and the versatility of the products, asymmetric total syntheses of indolizidine-alkaloids (-)-167B, (-)-195H, (-)-209D and (-)-223AB were accomplished.
Diastereopure Preparation of α-Benzotriazolyl 1-Azacycloalka[2,1-b] [1,3]-oxazines and their Application as Versatile Chiral Precursors
Xu, Xuenong,Lu, Jun,Li, Rui,Ge, Zongming,Dong, Yanmei,Hu, Yuefei
, p. 122 - 124 (2007/10/03)
A group of diastereopure α-benzotriazolyl 1-azacycloalka[2,1-b][1,3] oxazines were prepared from non-racemic Betti base and they were employed as the versatile precursors for the preparation of chiral ligands and chiral substituted azacyclics with signifi
