21794-66-1 Usage
Description
(1S)-1,5-anhydro-1-(1,6,7-trihydroxy-3-methoxy-9-oxo-9H-xanthen-2-yl)-D-glucitol is a complex organic compound that features a xanthen-2-yl moiety attached to a D-glucitol molecule. The xanthen-2-yl group is a heterocyclic ring with hydroxy and methoxy substituents, and the D-glucitol is a sugar alcohol. (1S)-1,5-anhydro-1-(1,6,7-trihydroxy-3-methoxy-9-oxo-9H-xanthen-2-yl)-D-glucitol is known for its potential biological activities, largely due to the presence of the xanthen-2-yl group, which is a common structural element in natural products and pharmaceuticals. Further research is necessary to fully understand its specific properties and potential applications.
Uses
Used in Pharmaceutical Industry:
(1S)-1,5-anhydro-1-(1,6,7-trihydroxy-3-methoxy-9-oxo-9H-xanthen-2-yl)-D-glucitol is used as a potential pharmaceutical agent for its possible biological activities. The xanthen-2-yl group, which is a part of its structure, is known to be present in certain natural products and pharmaceuticals, suggesting that this compound could have therapeutic applications once its specific properties are fully explored and understood.
Used in Research and Development:
In the field of scientific research, (1S)-1,5-anhydro-1-(1,6,7-trihydroxy-3-methoxy-9-oxo-9H-xanthen-2-yl)-D-glucitol serves as a subject for further study. Its complex structure and the presence of the xanthen-2-yl group make it an interesting candidate for exploring new chemical reactions, synthesis methods, and potential applications in various fields, including medicine and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 21794-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,9 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21794-66:
(7*2)+(6*1)+(5*7)+(4*9)+(3*4)+(2*6)+(1*6)=121
121 % 10 = 1
So 21794-66-1 is a valid CAS Registry Number.
21794-66-1Relevant articles and documents
Total synthesis of mangiferin, homomangiferin, and neomangiferin
Wei, Xiong,Liang, Danlin,Wang, Qing,Meng, Xiangbao,Li, Zhongjun
, p. 8821 - 8831 (2016/10/03)
Total synthesis of mangiferin, homomangiferin, and neomangiferin, three C-glycosyl xanthone natural products with a wide spectrum of pharmacological effects, has been achieved starting from 2,3,4,6-tetra-O-benzyl-α/β-d-glucopyranose. The key steps involve a stereoselective Lewis acid promoted C-glycosylation of protected phloroglucinol with tetrabenzylglucopyranosyl acetate and a highly regioselective base-induced cyclization for the construction of the core xanthone skeleton.
Synthesis of mangiferin, isomangiferin, and homomangiferin
Wu, Zhongtao,Wei, Guo,Lian, Gaoyan,Yu, Biao
supporting information; experimental part, p. 5725 - 5728 (2010/10/03)
Mangiferin, isomangiferin, and homomangiferin, the xanthone C-glycosides with a wide spectrum of pharmacological effects, were synthesized concisely, featuring a C-glycosylation of a xanthene derivative with perbenzylglucopyranosyl N-phenyltrifluoroacetimidate.
