CAS 652979-92-5

1,3-Dioxan-5-ol,4-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-phenyl-, (2S,4R,5R)-

Description:

1,3-Dioxan-5-ol, 4-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-phenyl-, (2S,4R,5R)- is a complex organic compound characterized by its dioxane ring structure, which features two oxygen atoms in a six-membered ring. This compound includes a hydroxyl group (-OH) at the 5-position, contributing to its potential as an alcohol. The presence of a phenyl group at the 2-position enhances its aromatic characteristics, while the tert-butyl dimethylsilyl group at the 4-position provides steric bulk and can influence its reactivity and solubility. The specific stereochemistry indicated by the (2S,4R,5R) configuration suggests that the compound has defined spatial arrangements of its substituents, which can significantly affect its chemical behavior and interactions. This compound may be of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals or as an intermediate in various chemical reactions. Its unique structure may also impart specific physical properties, such as solubility in organic solvents and potential applications in material science.

Formula: C₁₇H₂₈O₄Si

1,3-O-Benzylidene-4-O-t-butyl-dimethylsilyl-D-threitol

CAS: 652979-92-5

1,3-O-Benzylidene-4-O-t-butyl-dimethylsilyl-D-threitol is a synthetic carbohydrate that is structurally similar to D-threitol. It has a molecular weight of 323.07 and it has a melting point of 210°C. The CAS number for this compound is 652979-92-5. This compound has been modified with fluorination, methylation, and click chemistry. 1,3-O-Benzylidene-4-O-t -butyl dimethylsilyl D threitol has been used as a substrate for glycosylation reactions with oligosaccharides and polysaccharides in order to produce complex carbohydrates.

Formula: C₁₇H₂₈O₄Si

Purity: Min. 95%

Molecular weight: 324.49 g/mol

Ref: 3D-MB46624