53275-53-9

Usage

Uses

Used in Pharmaceutical Industry:
(3AS,4R,5S,6AR)-5-(BENZOYLOXY)HEXAHYDRO-4-(HYDROXYMETHYL)-2H-CYCLOPENTA[B]FURAN-2-ONE is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique structure allows it to be a key component in the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, (3AS,4R,5S,6AR)-5-(BENZOYLOXY)HEXAHYDRO-4-(HYDROXYMETHYL)-2H-CYCLOPENTA[B]FURAN-2-ONE serves as a valuable compound for studying its chemical properties, reactivity, and potential interactions with other molecules. This can lead to a better understanding of its applications and the development of new chemical processes.
Used in Synthesis of Prostaglandin Analogues:
(3AS,4R,5S,6AR)-5-(BENZOYLOXY)HEXAHYDRO-4-(HYDROXYMETHYL)-2H-CYCLOPENTA[B]FURAN-2-ONE is used as a key intermediate in the preparation of prostaglandin analogues. These analogues are important in the development of vasoactive drugs and EP4 receptor agonists, which have various medical applications, including the treatment of cardiovascular diseases and inflammation.
Used in Drug Delivery Systems:
Similar to gallotannin, (3AS,4R,5S,6AR)-5-(BENZOYLOXY)HEXAHYDRO-4-(HYDROXYMETHYL)-2H-CYCLOPENTA[B]FURAN-2-ONE can be employed in the development of novel drug delivery systems. These systems aim to improve the compound's delivery, bioavailability, and therapeutic outcomes by utilizing various organic and metallic nanoparticles as carriers.

InChI:InChI=1/C15H16O5/c16-8-11-10-6-14(17)19-12(10)7-13(11)20-15(18)9-4-2-1-3-5-9/h1-5,10-13,16H,6-8H2/t10-,11-,12?,13?/m1/s1

Downstream Products

• 70347-50-1 Benzoic acid (2R,3aR,6aS)-1-hydroxymethyl-5-oxo-octahydro-pentalen-2-yl ester 
• 81266-59-3 Benzoic acid (3aR,5R,6aS)-4-(tert-butyl-dimethyl-silanyloxymethyl)-2-[1-ethoxycarbonyl-meth-(E)-ylidene]-hexahydro-cyclopenta[b]furan-5-yl ester 
• 81266-62-8 Benzoic acid (2R,3aR,6aS)-1-(tert-butyl-dimethyl-silanyloxymethyl)-5-oxo-octahydro-pentalen-2-yl ester 
• 81266-61-7 (3aS,5R,6aR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-5-hydroxy-hexahydro-pentalen-2-one 
• 64982-34-9 Benzoic acid (3aR,5R,6aS)-4-(tert-butyl-dimethyl-silanyloxymethyl)-2-oxo-hexahydro-cyclopenta[b]furan-5-yl ester 

Relevant academic research and scientific papers

One-pot method of preparing benzoyl the branch stands lactone (by machine translation)

The present invention discloses a one-pot method for preparing benzoyl the branch stands lactone. At the same in the reaction container, to the branch stands lactone diol as raw materials, adding solvent S1 And triphenyl methyl chloride to primary hydroxyl position of the alkylation reaction, to obtain [...] lactone solvent S [...] hydroxy derivatives1 The reaction system, benzoyl chloride to continue adding hydroxyl position of acylation reaction, and adding solvent S2 , Recrystallization, get the branch stands lactone glycol double-hydroxy derivative; adding solvent S3 And acid solution hydrolysis reaction of the primary hydroxyl group position, make the branch stands lactone crude benzoyl; adding solvent S4 Or/and S5 , Recrystallization, disposable and preparing the corresponding optically active benzoyl the branch stands lactone. The invention avoid each step reaction is repeatedly re-feeding the tedious; adequate reaction, little side reaction, high purity; after treatment is simple, high yield; and the operation is simple, time saving and high efficiency, saving the material, reducing the cost, and is suitable for industrial production. (by machine translation)