The chemical substance with the name "[(5S,6R,7R,8S)-6-acetoxy-3,3-dimethyl-8-(p-tolylsulfonyloxy)-2,4,10-trioxaspiro[4.5]decan-7-yl] acetate" and CAS number 53821-66-2 is a complex organic compound characterized by its spirocyclic structure, which includes multiple functional groups such as acetoxy and sulfonyloxy moieties. This compound features a spirodecane framework, indicating a unique three-dimensional arrangement that can influence its reactivity and biological activity. The presence of stereocenters (5S, 6R, 7R, 8S) suggests that it may exhibit chirality, potentially leading to different optical isomers with varying properties. The acetoxy groups contribute to its reactivity, making it a candidate for various chemical transformations. Additionally, the p-tolylsulfonyloxy group enhances its solubility and may improve its pharmacological profile. Overall, this compound's intricate structure and functional groups suggest potential applications in medicinal chemistry, particularly in the development of therapeutics or as intermediates in organic synthesis.

[(5S,6R,7R,8S)-6-acetoxy-3,3-dimethyl-8-(p-tolylsulfonyloxy)-2,4,10-trioxaspiro[4.5]decan-7-yl] acetate

53821-66-2: The chemical substance with the name "[(5S,6R,7R,8S)-6-acetoxy-3,3-dimethyl-8-(p-tolylsulfonyloxy)-2,4,10-trioxaspiro[4.5]decan-7-yl] acetate" and CAS number 53821-66-2 is a complex organic compound characterized by its spirocyclic structure, which includes multiple functional groups such as acetoxy and sulfonyloxy moieties. This compound features a spirodecane framework, indicating a unique three-dimensional arrangement that can influence its reactivity and biological activity. The presence of stereocenters (5S, 6R, 7R, 8S) suggests that it may exhibit chirality, potentially leading to different optical isomers with varying properties. The acetoxy groups contribute to its reactivity, making it a candidate for various chemical transformations. Additionally, the p-tolylsulfonyloxy group enhances its solubility and may improve its pharmacological profile. Overall, this compound's intricate structure and functional groups suggest potential applications in medicinal chemistry, particularly in the development of therapeutics or as intermediates in organic synthesis.

3,4-Di-O-acetyl-1,2-O-isopropylidene-5-O-tosyl-α-L-sorbose

<p>3,4-Di-O-acetyl-1,2-O-isopropylidene-5-O-p-toluenesulfonyl-a-L-sorbopyranose is a fluorinated glycosylation product with a synthetic route. It is a high purity custom synthesis and can be modified according to customer needs. 3,4-Di-O-acetyl-1,2-O isopropylidene -5 O p toluenesulfonyl A L sorbopyranose has been used in the synthesis of oligosaccharides and saccharides.</p>

CAS 53821-66-2

[(5S,6R,7R,8S)-6-acetoxy-3,3-dimethyl-8-(p-tolylsulfonyloxy)-2,4,10-trioxaspiro[4.5]decan-7-yl] acetate

3,4-Di-O-acetyl-1,2-O-isopropylidene-5-O-tosyl-α-L-sorbose

Ref: 7W-GC0564

3,4-Di-O-acetyl-1,2-O-isopropylidene-5-O-p-toluenesulfonyl-a-L-sorbopyranose

Ref: 3D-MD04661