55740-45-9 Usage
Description
[4,8-Dimethoxyfuro[2,3-b]quinolin-7-yl]6-deoxy-α-L-mannopyranoside is a glycosidic alkaloid of the furanoquinoline type, which is found in the extract from Haplophyllum perforatum. Its structure has been established through the study of infrared, ultraviolet, NMR, and mass spectra.
Uses
Used in Pharmaceutical Industry:
[4,8-Dimethoxyfuro[2,3-b]quinolin-7-yl]6-deoxy-α-L-mannopyranoside is used as a pharmaceutical compound for its potential therapeutic properties. As a glycosidic alkaloid, it may exhibit bioactive properties that can be harnessed for the development of new drugs or treatments.
Used in Research and Development:
[4,8-Dimethoxyfuro[2,3-b]quinolin-7-yl]6-deoxy-α-L-mannopyranoside is used as a research compound for studying the chemical properties and potential applications of furanoquinoline alkaloids. Its unique structure and the fact that it has been characterized through various spectroscopic methods make it an interesting subject for further investigation in the fields of chemistry and biology.
References
Akhrnedzhanova, Bessonova, Yunusov, Khim. Prir. Soedin., 10, 680 (1974)
Check Digit Verification of cas no
The CAS Registry Mumber 55740-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,4 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55740-45:
(7*5)+(6*5)+(5*7)+(4*4)+(3*0)+(2*4)+(1*5)=129
129 % 10 = 9
So 55740-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H21NO8/c1-8-13(21)14(22)15(23)19(27-8)28-11-5-4-9-12(17(11)25-3)20-18-10(6-7-26-18)16(9)24-2/h4-8,13-15,19,21-23H,1-3H3/t8-,13-,14+,15+,19-/m0/s1
55740-45-9Relevant articles and documents
HAPLOSININE - A NEW FURANOQUINOLINE GLYCOALKALOID FROM Haplophyllum perforatum
Rasulova, Kh. A.,Bessonova, I. A.,Yagudaev, M. R.,Yunusov, S. Yu.
, p. 731 - 734 (2007/10/02)
The new glycoalkaloid haplosinine has been isolated from the epigeal part of Haplophyllum perforatum (M.B.) Kar. et Kir., and its structure has been established on the basis of chemical transformations and a comparative analysis of its 13C NMR spectra with those of known compounds as haplopine 7-O-3)-α-L-rhamnopyranoside>.
