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The chemical compound "(3aR,4R,5R,6aS)-4-[(E)-4-(3-Chloro-phenoxy)-3-hydroxy-but-1-enyl]-5-hydroxy-hexahydro-cyclopenta[b]furan-2-one" is a complex organic molecule with a unique structure. It features a cyclopenta[b]furan-2-one core, which is a five-membered ring fused to a furan ring. The molecule has a hexahydro structure, indicating the presence of six hydrogen atoms bonded to carbon in a cyclic manner. A key functional group in (3aR,4R,5R,6aS)-4-[(E)-4-(3-Chloro-phenoxy)-3-hydroxy-but-1-enyl]-5-hydroxy-hexahydro-cyclopenta[b]furan-2-one is the (E)-4-(3-chlorophenoxy)-3-hydroxybut-1-enyl moiety, which includes a chlorophenoxy group attached to a hydroxybutenyl chain. This group is connected to the cyclopenta[b]furan-2-one core, contributing to the molecule's overall reactivity and potential applications. The compound's stereochemistry is defined by the (3aR,4R,5R,6aS) configuration, which specifies the three-dimensional arrangement of atoms around the asymmetric centers. This specific arrangement can significantly influence the compound's physical and chemical properties, as well as its potential biological activity.

52267-81-9

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52267-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52267-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,6 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52267-81:
(7*5)+(6*2)+(5*2)+(4*6)+(3*7)+(2*8)+(1*1)=119
119 % 10 = 9
So 52267-81-9 is a valid CAS Registry Number.

52267-81-9Relevant academic research and scientific papers

PROSTANOIDS. XXVII. SOME ASPECTS OF CHEMO- AND STEREOSELECTIVE REDUCTION OF 7α-HYDROXY-6β-(3-OXO-4-m-CHLOROPHENOXY-1E-BUTENYL)-2-OXABICYCLOOCTAN-3-ONE

Miftakhov, M. S.,Vostrikov, N. S.,Kuznetsov, O. M.,Singizova, V. R.,Kuchin, A. V.,Tolstikov, G. A.

, p. 851 - 856 (2007/10/02)

The chemoselective reduction of 7α-hydroxy-6β-(3-oxo-4-m-chlorophenoxy-1E-butenyl)-2-oxabicyclooctan-3-one with respect to the oxo group was studied by means of readily obtainable reagents based on boron and aluminum.The optimum stereoselectivity of reduction was obtained with the use of diisobutylaluminum 2,6-di-tert-butyl-4-methylphenoxide in methylene chloride at -78 deg C.

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