1,1-Dimethylethyl-(R,S)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate, with the CAS number 127589-93-9, is a chemical compound characterized by its oxazolidine structure, which incorporates both a formyl group and a carboxylate moiety. This compound features a chiral center, indicated by the (R,S) designation, suggesting that it exists as a racemic mixture of enantiomers. The presence of the dimethyl groups contributes to its steric bulk, influencing its reactivity and interactions with other molecules. The oxazolidine ring is known for its stability and is often utilized in organic synthesis and medicinal chemistry due to its ability to participate in various chemical reactions, including nucleophilic attacks and cycloadditions. Additionally, the formyl group can serve as a reactive site for further functionalization, making this compound potentially valuable in the synthesis of more complex organic molecules. Its specific applications and properties would depend on the context of its use in research or industry, particularly in the fields of pharmaceuticals or agrochemicals.

1,1-dimethylethyl-(R,S)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate

127589-93-9: 1,1-Dimethylethyl-(R,S)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate, with the CAS number 127589-93-9, is a chemical compound characterized by its oxazolidine structure, which incorporates both a formyl group and a carboxylate moiety. This compound features a chiral center, indicated by the (R,S) designation, suggesting that it exists as a racemic mixture of enantiomers. The presence of the dimethyl groups contributes to its steric bulk, influencing its reactivity and interactions with other molecules. The oxazolidine ring is known for its stability and is often utilized in organic synthesis and medicinal chemistry due to its ability to participate in various chemical reactions, including nucleophilic attacks and cycloadditions. Additionally, the formyl group can serve as a reactive site for further functionalization, making this compound potentially valuable in the synthesis of more complex organic molecules. Its specific applications and properties would depend on the context of its use in research or industry, particularly in the fields of pharmaceuticals or agrochemicals.

3-Oxazolidinecarboxylic acid, 4-formyl-2,2-dimethyl-, 1,1-dimethylethyl ester

1,1-Dimethylethyl 4-formyl-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

CAS 127589-93-9

1,1-dimethylethyl-(R,S)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate

3-Oxazolidinecarboxylic acid, 4-formyl-2,2-dimethyl-, 1,1-dimethylethyl ester

Ref: IN-DA000X6H

1,1-Dimethylethyl 4-formyl-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

Ref: 54-OR92245

tert-Butyl 4-formyl-2,2-dimethyloxazolidine-3-carboxylate

Ref: 10-F233709