CAS 131233-89-1: (2S,4R)-2-(tert-Butyl)-3-formyl-4-oxazolidinecarboxylic Acid Methyl Ester

Description: (2S,4R)-2-(tert-Butyl)-3-formyl-4-oxazolidinecarboxylic Acid Methyl Ester is a chiral compound characterized by its oxazolidine ring structure, which contributes to its stereochemistry and potential biological activity. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The formyl group introduces a reactive aldehyde functionality, which can participate in various chemical reactions, including condensation and reduction. The methyl ester moiety provides a means for further functionalization and can influence the compound's reactivity and stability. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for research in medicinal chemistry. Additionally, its stereochemical configuration is crucial for its interaction with biological targets, potentially affecting its efficacy and safety profile. Overall, this compound's unique characteristics make it a valuable subject for further study in synthetic and medicinal chemistry.

Formula: C₁₀H₁₇NO₄

Synonyms:

• (2S,-cis)-2-(1,1-Diomethylethyl)-3-formyl-4-oxazolidinecarboxylic Acid Methyl Ester

4-Oxazolidinecarboxylic acid, 2-(1,1-dimethylethyl)-3-formyl-, methyl ester, (2S,4R)-

CAS: 131233-89-1

• Formula: C₁₀H₁₇NO₄
• Color and Shape: Solid
• Molecular weight: 215.2463

(2S,4R)-2-(tert-Butyl)-3-formyl-4-oxazolidinecarboxylic acid methyl ester

CAS: 131233-89-1

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• Formula: C₁₀H₁₇NO₄
• Purity: Min. 95%
• Molecular weight: 215.25 g/mol