197631-20-2 Usage
Description
(2Z,3E,5E,7E,9E,11E,13E)-14-[(7S,8R,9R)-7,8-dihydroxy-5-oxo-9-(1,2,3-trihydroxypropyl)-4,10-dioxabicyclo[4.4.0]deca-2,11-dien-3-yl]-2-(2,4-dimethylhexylidene)-4-methyl-tetradeca-3,5,7,9,11,13-hexaenoic acid is a complex fatty acid derivative characterized by a long carbon chain with multiple double bonds and functional groups. The presence of dihydroxy and trihydroxypropyl groups suggests potential biological activity and the ability to bind to specific receptors in living organisms. Its chemical structure indicates possible applications in biochemistry, pharmaceuticals, and biotechnology research.
Uses
Used in Biochemistry Research:
(2Z,3E,5E,7E,9E,11E,13E)-14-[(7S,8R,9R)-7,8-dihydroxy-5-oxo-9-(1,2,3-trihydroxypropyl)-4,10-dioxabicyclo[4.4.0]deca-2,11-dien-3-yl]-2-(2,4-dimethylhexylidene)-4-methyl-tetradeca-3,5,7,9,11,13-hexaenoic acid is used as a research compound for studying its interactions with biological molecules and understanding its potential role in biochemical processes.
Used in Pharmaceutical Development:
This complex molecule is used in the development of pharmaceuticals, where its unique structure and functional groups may contribute to the design of new drugs with specific targeting or therapeutic properties.
Used in Biotechnology Applications:
(2Z,3E,5E,7E,9E,11E,13E)-14-[(7S,8R,9R)-7,8-dihydroxy-5-oxo-9-(1,2,3-trihydroxypropyl)-4,10-dioxabicyclo[4.4.0]deca-2,11-dien-3-yl]-2-(2,4-dimethylhexylidene)-4-methyl-tetradeca-3,5,7,9,11,13-hexaenoic acid is utilized in biotechnology for exploring its potential in the creation of novel bioactive molecules or as a component in bioengineering projects.
Check Digit Verification of cas no
The CAS Registry Mumber 197631-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,6,3 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 197631-20:
(8*1)+(7*9)+(6*7)+(5*6)+(4*3)+(3*1)+(2*2)+(1*0)=162
162 % 10 = 2
So 197631-20-2 is a valid CAS Registry Number.
InChI:InChI=1/C34H44O10/c1-5-21(2)16-23(4)18-24(33(40)41)17-22(3)14-12-10-8-6-7-9-11-13-15-25-19-27-28(34(42)43-25)30(38)31(39)32(44-27)29(37)26(36)20-35/h6-15,17-19,21,23,26,29-32,35-39H,5,16,20H2,1-4H3,(H,40,41)/b7-6+,10-8+,11-9+,14-12+,15-13+,22-17+,24-18-/t21?,23?,26?,29?,30-,31+,32-/m0/s1
197631-20-2Relevant articles and documents
Polyunsaturated C-Glycosidic 4-Hydroxy-2-pyrone Derivatives: Total Synthesis Shows that Putative Orevactaene Is Likely Identical with Epipyrone A
Preindl, Johannes,Schulthoff, Saskia,Wirtz, Conny,Lingnau, Julia,Fürstner, Alois
, p. 7525 - 7530 (2017)
Orevactaene and epipyrone A were previously thought to comprise the same polyunsaturated tail but notably different C-glycosylated 4-hydroxy-2-pyrone head groups. Total synthesis now shows that the signature bicyclic framework assigned to orevactaene is a chimera; the compound is almost certainly identical with epipyrone A, whose previously unknown stereochemistry has also been established during this study. Key to success was the ready formation of the bicyclic core of putative orevactaene by a sequence of two alkyne cycloisomerization reactions using tungsten and gold catalysis. Equally important was the flexibility in the assembly process gained by the use of heterobimetallic polyunsaturated modules whose termini could be selectively and consecutively addressed in a practical one-pot cross-coupling sequence.
