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CAS 153053-19-1

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1,1-Dimethylethyl (4R)-2,2-dimethyl-4-(2-oxoethyl)-3-oxazolidinecarboxylate

Description:
1,1-Dimethylethyl (4R)-2,2-dimethyl-4-(2-oxoethyl)-3-oxazolidinecarboxylate, with CAS number 153053-19-1, is a chemical compound characterized by its oxazolidine ring structure, which incorporates both ester and ketone functionalities. This compound features a chiral center, indicated by the (4R) designation, suggesting that it exists in a specific stereoisomeric form. The presence of the dimethyl groups contributes to its steric bulk, potentially influencing its reactivity and interactions with other molecules. The oxazolidine ring is known for its applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its ability to mimic amino acids and peptides. Additionally, the ester group may enhance solubility and bioavailability, making it a candidate for various chemical applications. Overall, the unique structural features of this compound suggest potential utility in synthetic organic chemistry and drug development, although specific applications would depend on further research into its properties and behavior in different environments.
Formula:C12H21NO4
InChI:InChI=1S/C12H21NO4/c1-11(2,3)17-10(15)13-9(6-7-14)8-16-12(13,4)5/h7,9H,6,8H2,1-5H3/t9-/m1/s1
InChI key:InChIKey=GAWRNYMYEGSVFV-SECBINFHSA-N
SMILES:C(C=O)[C@H]1N(C(OC(C)(C)C)=O)C(C)(C)OC1
Synonyms:
  • (4r)-2,2-Dimethyl-4-(2-oxoethyl)-oxazolidine-3-carboxylic acid tert-butyl ester
  • (R)-tert-Butyl2,2-dimethyl-4-(2-oxoethyl)oxazolidine-3-carboxylate
  • 3-Oxazolidinecarboxylic acid, 2,2-dimethyl-4-(2-oxoethyl)-, 1,1-dimethylethyl ester, (R)-
  • 1,1-Dimethylethyl (4R)-2,2-dimethyl-4-(2-oxoethyl)-3-oxazolidinecarboxylate
  • 3-Oxazolidinecarboxylic acid, 2,2-dimethyl-4-(2-oxoethyl)-, 1,1-dimethylethyl ester, (4R)-
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