64421-27-8 Usage
Uses
Given the provided materials, there are no specific applications listed for (1S,7S)-1-(β-D-Glucopyranosyloxy)-1,4aα,5,6,7,7aα-hexahydro-7-hydroxy-7-methylcyclopenta[c]pyran-4-carboxylic acid methyl ester. However, based on its structural features, one could hypothesize potential uses in various fields, pending further research and validation:
Used in Pharmaceutical Industry:
(1S,7S)-1-(β-D-Glucopyranosyloxy)-1,4aα,5,6,7,7aα-hexahydro-7-hydroxy-7-methylcyclopenta[c]pyran-4-carboxylic acid methyl ester could be used as a pharmaceutical agent for [specific therapeutic area] due to its complex structure and potential biological activity.
Used in Chemical Research:
In the field of chemical research, (1S,7S)-1-(β-D-Glucopyranosyloxy)-1,4aα,5,6,7,7aα-hexahydro-7-hydroxy-7-methylcyclopenta[c]pyran-4-carboxylic acid methyl ester could serve as a subject for studying the effects of stereochemistry on biological activity and interactions with biological targets.
Used in Material Science:
(1S,7S)-1-(β-D-Glucopyranosyloxy)-1,4aα,5,6,7,7aα-hexahydro-7-hydroxy-7-methylcyclopenta[c]pyran-4-carboxylic acid methyl ester might also be explored for its potential use in the development of new materials, given its unique structural elements.
Check Digit Verification of cas no
The CAS Registry Mumber 64421-27-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,2 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64421-27:
(7*6)+(6*4)+(5*4)+(4*2)+(3*1)+(2*2)+(1*7)=108
108 % 10 = 8
So 64421-27-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H26O10/c1-17(23)4-3-7-8(14(22)24-2)6-25-15(10(7)17)27-16-13(21)12(20)11(19)9(5-18)26-16/h6-7,9-13,15-16,18-21,23H,3-5H2,1-2H3/t7-,9-,10-,11-,12+,13-,15+,16+,17+/m1/s1
64421-27-8Relevant academic research and scientific papers
IRIDOID GLUCOSIDES IN AVICENNIA MARINA
Koenig, Gabriele,Rimpler, Horst
, p. 1245 - 1248 (2007/10/02)
Key Word Index - Avicennia marina; Verbenaceae; iridoids; geniposidic acid; mussaenosidic acid; 2'-cinnamoylmussaenosidic acid; 10-O-(5-phenyl-2,4-pentadienoyl)-geniposidic acid; 7-O-(5-phenyl-2,4-pentadienoyl)-8-epiloganic acid. - 2'-Cinnamoyl-mussaenoside , 10-O-(5-phenyl-2,4-pentadienoyl)-geniposide, 7-O-(5-phenyl-2,4-pentadienoyl)-8-epiloganin, and the known iridoids geniposide and mussaenoside have been isolated from a methylated extract of the leaves of Avicennia marina.Evidence is presented that the iridoids occur as the free acids in the plant.The taxonomic significance of these findings is discussed.
Ladroside (=6'-Caffeoyl-mussaenoside), a New Iridoid Glucoside from Veronica officinalis L. (Scrophulariaceae) and the Elucidation of the Absolute Configuration at C(8) of Mussaenoside
Affifi-Yazar, Fatma Ue.,Sticher, Otto,Uesato, Shinichi,Nagajima, Kimiko,Inouye, Hiroyuki
, p. 16 - 24 (2007/10/02)
A new iridoid glucoside, named ladroside, together with mussaenoside (1) , has been isolated from Veronica officialis L.The structure of ladroside (4) and the identity of mussaenoside have been established by spectral analysis.Additionally, the absolute configuration at C(8) carrying hydroxyl group has been established by chemical evidence.
