22487-36-1 Usage
Uses
Used in Organic Chemistry:
(1R,2S,6S,9S)-9-methyl-2-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-oxabicyclo[4.3.0]non-4-ene-5-carboxylic acid is used as a complex molecule for studying its chemical reactivity and potential applications in organic synthesis.
Used in Biochemistry:
(1R,2S,6S,9S)-9-methyl-2-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-oxabicyclo[4.3.0]non-4-ene-5-carboxylic acid is used as a compound of interest for investigating its potential biological activity and interactions with biomolecules.
Used in Pharmaceutical Research:
(1R,2S,6S,9S)-9-methyl-2-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-oxabicyclo[4.3.0]non-4-ene-5-carboxylic acid is used as a candidate for drug development due to its intricate structure and potential activity in various therapeutic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 22487-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,8 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22487-36:
(7*2)+(6*2)+(5*4)+(4*8)+(3*7)+(2*3)+(1*6)=111
111 % 10 = 1
So 22487-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H24O9/c1-6-2-3-7-8(14(21)22)5-23-15(10(6)7)25-16-13(20)12(19)11(18)9(4-17)24-16/h5-7,9-13,15-20H,2-4H2,1H3,(H,21,22)/t6-,7+,9-,10+,11-,12+,13-,15-,16+/m1/s1
22487-36-1Relevant academic research and scientific papers
Iridoid glucosides from Picconia excelsa
Damtoft, Soren,Franzyk, Henrik,Jensen, Soren Rosendal
, p. 743 - 750 (2007/10/03)
An investigation of the iridoids of Picconia excelsa from Tenerife provided 17 iridoid glucosides together with verbascoside. Major constituents (> 0.5%) were loganin, ketologanin, oleoacteoside and the new picconioside I- a bisiridoid consisting of loganin esterified with deoxyloganin. Minor constituents were secoxyloganin, 8-epi-kingiside, oleoside 11-methyl ester, excelsioside, ligstroside and loganic acid together with the new compounds ketologanic acid, 6β-hydroxy-7-epi-loganin and picconiosides II-V, the latter four being esters of loganin and menthiafolic, foliamenthic, 6-(Z)- foliamenthic or 6,7-dihydrofoliamenthic acid. The structures were mainly elucidated by NMR spectroscopy.
