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CAS 169032-99-9

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(2S,4S)-1-tert-butyl 2-methyl 4-chloropyrrolidine-1,2-dicarboxylate

Description:
(2S,4S)-1-tert-butyl 2-methyl 4-chloropyrrolidine-1,2-dicarboxylate is a chiral compound characterized by its pyrrolidine ring structure, which contains two carboxylate functional groups and a tert-butyl group. The presence of the chlorine atom at the 4-position of the pyrrolidine ring contributes to its unique reactivity and potential biological activity. This compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its chirality, indicated by the (2S,4S) configuration, suggests that it may exhibit specific interactions in biological systems, making it of interest in medicinal chemistry. The dicarboxylate nature of the molecule allows for various chemical modifications, enhancing its versatility in synthetic applications. Additionally, the tert-butyl group provides steric hindrance, which can influence the compound's solubility and reactivity. Overall, this compound exemplifies the complexity and utility of chiral molecules in chemical research and development.
Formula:C11H18ClNO4
InChI:InChI=1/C11H18ClNO4/c1-11(2,3)17-10(15)13-6-7(12)5-8(13)9(14)16-4/h7-8H,5-6H2,1-4H3/t7-,8-/m0/s1
SMILES:CC(C)(C)OC(=O)N1C[C@H](C[C@H]1C(=O)OC)Cl
Synonyms:
  • 1,2-pyrrolidinedicarboxylic acid, 4-chloro-, 1-(1,1-dimethylethyl) 2-methyl ester, (2S,4S)-
  • 1-tert-Butyl 2-methyl (2S,4S)-4-chloropyrrolidine-1,2-dicarboxylate
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