CAS 226214-50-2

3,6-Dioxabicyclo[3.2.1]octane-5-methanol,7-methoxy-8-(phenylmethoxy)-, (1R,5S,7S,8S)-

Description:

3,6-Dioxabicyclo[3.2.1]octane-5-methanol, 7-methoxy-8-(phenylmethoxy)-, with the CAS number 226214-50-2, is a complex organic compound characterized by its bicyclic structure, which includes two ether linkages (dioxabicyclo) and multiple functional groups. The presence of methanol and methoxy groups indicates that it has hydroxyl (-OH) and methoxy (-OCH3) functionalities, which can influence its solubility and reactivity. The phenylmethoxy group suggests that the compound may exhibit aromatic characteristics, potentially affecting its electronic properties and interactions with other molecules. The stereochemistry indicated by the (1R,5S,7S,8S) notation implies specific spatial arrangements of atoms, which can significantly impact the compound's biological activity and chemical behavior. Such compounds may be of interest in medicinal chemistry or materials science due to their unique structural features and potential applications. However, detailed studies would be necessary to fully understand its properties, reactivity, and potential uses in various fields.

Formula: C₁₅H₂₀O₅

(1S,3S,4R,8S)-8-Benzyloxy-1-hydroxymethyl-3-methoxy-2,6-dioxabicyclo[3,2,1]octane

CAS: 226214-50-2

1-Hydroxymethyl-8-benzyloxy-3-methoxy-2,6-dioxabicyclo[3,2,1]octane is a sugar that can be modified with various functional groups. This compound is synthesized by modification of the 1S,3S,4R,8S configuration of 8-Benzyloxy-1-(hydroxymethyl)-3-methoxy-2,6 dioxabicyclo[3,2,1]octane. The synthesis can be performed in two steps: first the hydroxymethyl group is replaced by benzyloxymethyl using 1-(benzyloxy)propanol and then the methoxy group is replaced by a methoxy group with sodium methoxide.

Formula: C₁₅H₂₀O₅

Purity: Min. 95%

Molecular weight: 280.32 g/mol

Ref: 3D-MB10613