131435-06-8 Usage
Description
(+)-EPI-QUERCITOL is a stereoisomer of the naturally occurring flavonol quercitol, characterized by its polyhydroxy compound nature and a specific chemical structure with a unique spatial arrangement of atoms. Found in certain plants and natural sources, this compound has garnered attention for its potential pharmaceutical and therapeutic applications. Its distinctive chemical properties position it as a promising candidate in drug research and development, as well as in the study of natural products and their biological activities.
Uses
Used in Pharmaceutical Research and Development:
(+)-EPI-QUERCITOL is utilized as a subject of interest in pharmaceutical research and development due to its unique chemical properties and potential therapeutic applications. Its presence in natural sources and plants makes it a valuable compound for exploring new avenues in medicine and healthcare.
Used in the Study of Natural Products and Biological Activities:
(+)-EPI-QUERCITOL serves as a key component in the study of natural products and their biological activities. Its multiple hydroxyl groups and specific chemical structure contribute to its potential role in various scientific and technological applications, warranting further research to uncover its full range of benefits and uses.
Check Digit Verification of cas no
The CAS Registry Mumber 131435-06-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,4,3 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 131435-06:
(8*1)+(7*3)+(6*1)+(5*4)+(4*3)+(3*5)+(2*0)+(1*6)=88
88 % 10 = 8
So 131435-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O5/c7-2-1-3(8)5(10)6(11)4(2)9/h2-11H,1H2/t2-,3+,4-,5-,6-/m0/s1
131435-06-8Relevant articles and documents
Stereoselective syntheses of racemic quercitols and bromoquercitols starting from cyclohexa-1,4-diene: Gala-, epi-, muco-, and neo-quercitol
Aydin, G?kay,Savran, Tahir,Akta?, Fatih,Baran, Arif,Balci, Metin
, p. 1511 - 1524 (2013/05/21)
The efficient synthesis of gala-, epi-, neo-, and muco-quercitols and some brominated quercitols starting from cyclohexa-1,4-diene is reported. Treatment of the dibromide, obtained by the addition of bromine to cyclohexa-1,4-diene, with m-chloroperbenzoic
Highly stereoselective and stereospecific syntheses of a variety of quercitols from d-(-)-quinic acid
Shih, Tzenge-Lien,Lin, Ya-Ling,Kuo, Wei-Shen
, p. 1919 - 1924 (2007/10/03)
The highly stereoselective synthesis of (-)-epi-, (-)-allo- and neo-quercitols as well as stereospecific synthesis of (-)-talo- and (+)-gala-quercitols have been achieved. The general strategy is employing dihydroxylation of the isolated double bond of various kinds of protected chiral (1,4,5)-cyclohex-2-ene-triols, which are derived from d-(-)-quinic acid. The choosing of protecting groups from either BBA (butane 2,3-bisacetal) or acetyl groups will result in the various degrees of stereoselectivity of dihydroxylation. On the other hand, the cyclohexylidene acetal moiety is attributed to the stereospecificity during dihydroxylation to afford the request molecules.
Synthesis of the enantiomers of 6-deoxy-myo-inositol 1,3,4,5-Tetrakisphosphate, structural analogues of myo-inositol 1,3,4,5-Tetrakisphosphate
Horne, Graeme,Potter, Barry V. L.
, p. 80 - 87 (2007/10/03)
D-myo-Inositol 1,3,4,5-tetrakisphosphate [Ins(1,3,4,5)P4] is produced rapidly from the established second messenger D-myo-inositol 1,4,5trisphosphate [Ins(1,4,5)P4] in stimulated cells. Despite extensive investigations, in particular
