7344-47-0 Usage
Uses
Used in Pharmaceutical Industry:
(11S)-15,17-dihydroxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-15,17,19-trien-13-one could be used as a pharmaceutical agent for [specific medical condition or treatment] due to its complex structure and potential reactivity, which may allow it to interact with biological targets.
Used in Chemical Research:
In the field of chemical research, (11S)-15,17-dihydroxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-15,17,19-trien-13-one might serve as a model compound for studying the effects of bicyclic structures and hydroxyl group placements on molecular properties and reactivity.
Used in Material Science:
(11S)-15,17-dihydroxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-15,17,19-trien-13-one could be explored for its potential use in the development of new materials, such as polymers or coatings, that leverage its unique structural features and reactive sites.
Without specific applications provided in the materials, these uses are speculative and would need to be investigated through scientific research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 7344-47-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,4 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7344-47:
(6*7)+(5*3)+(4*4)+(3*4)+(2*4)+(1*7)=100
100 % 10 = 0
So 7344-47-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H26O4/c1-13-9-7-5-3-2-4-6-8-10-14-11-15(19)12-16(20)17(14)18(21)22-13/h11-13,19-20H,2-10H2,1H3/t13-/m0/s1
7344-47-0Relevant academic research and scientific papers
Cu(I)-catalyzed macrocyclic Sonogashira-type cross-coupling
Santandrea, Jeffrey,Bedard, Anne-Catherine,Collins, Shawn K.
supporting information, p. 3892 - 3895 (2014/08/18)
A macrocyclic Cu-catalyzed Sonogashira-type cross-coupling reaction has been developed that employs an operationally simple CuCl/phen/Cs 2CO3 catalyst system. Macrocyclizations can be performed at relatively high concentrations witho
The total synthesis of both enantiomers of the macrocyclic lactone zearalane
Bracher,Krauss
, p. 4701 - 4704 (2007/10/03)
A straightforward approach to both enantiomers of zearalane is described from the enantiomerically pure alkenol (S)-4, prepared by a kinetic enzymatic resolution of the racemate. The key step is a Pd-catalyzed cross-coupling of an arene trifluoromethanesulfonate with a 9-alkyl-9-borabicyclo-[3.3.1]nonane derivative. The two enantiomers 2a and 2b have been obtained in an enantiodivergent manner by macrolactonization of the hydroxy acid (S)-7 with either Gerlach's modification of the Corey lactonization or a Mitsunobu lactonization.
