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CAS 147266-79-3

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(2S,4S)-1-(TERT-BUTOXYCARBONYL)-4-PHENOXY-2-PYRROLIDINECARBOXYLIC ACID

Description:
(2S,4S)-1-(tert-Butoxycarbonyl)-4-phenoxy-2-pyrrolidinecarboxylic acid is a chiral compound characterized by its pyrrolidine ring structure, which features a tert-butoxycarbonyl (Boc) protecting group and a phenoxy substituent. This compound is typically used in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals due to its potential biological activity. The presence of the Boc group allows for selective deprotection under mild conditions, facilitating further functionalization of the molecule. The stereochemistry indicated by the (2S,4S) configuration suggests specific spatial arrangements of the substituents, which can significantly influence the compound's reactivity and interaction with biological targets. Additionally, the carboxylic acid functional group contributes to its acidity and potential for forming salts, enhancing its solubility in various solvents. Overall, this compound exemplifies the complexity and utility of chiral molecules in chemical research and development.
Formula:C16H21NO5
InChI:InChI=1/C16H21NO5/c1-16(2,3)22-15(20)17-10-12(9-13(17)14(18)19)21-11-7-5-4-6-8-11/h4-8,12-13H,9-10H2,1-3H3,(H,18,19)/t12-,13-/m0/s1
SMILES:CC(C)(C)OC(=O)N1C[C@H](C[C@H]1C(=O)O)Oc1ccccc1
Synonyms:
  • (2S,4S)-Boc-4-Phenoxy-Pyrrolidine-2-Carboxylic Acid
  • (2S,4S)-1-(Tert-Butoxycarbonyl)-4-Phenoxypyrrolidine-2-Carboxylic Acid
  • (2S,4S)-Boc-4-phenoxy-Pro-OH
  • (4S)-1-(tert-butoxycarbonyl)-4-phenoxy-L-proline
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