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CAS 117625-90-8

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1-Pyrrolidinecarboxylicacid, 2-formyl-, 1,1-dimethylethyl ester

Description:
1-Pyrrolidinecarboxylic acid, 2-formyl-, 1,1-dimethylethyl ester, commonly referred to by its CAS number 117625-90-8, is an organic compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. This compound features a carboxylic acid functional group and an ester linkage, indicating it can participate in various chemical reactions typical of esters, such as hydrolysis and transesterification. The presence of a formyl group suggests it may exhibit reactivity associated with aldehydes, including potential condensation reactions. The tert-butyl ester group enhances its lipophilicity, making it more soluble in organic solvents, which can be advantageous in synthetic applications. Additionally, the compound may exhibit biological activity, as many pyrrolidine derivatives are known for their pharmacological properties. Its stability, reactivity, and solubility characteristics make it a valuable intermediate in organic synthesis and medicinal chemistry. However, specific applications and biological effects would require further investigation and context.
Formula:C10H17NO3
InChI:InChI=1S/C10H17NO3/c1-10(2,3)14-9(13)11-6-4-5-8(11)7-12/h7-8H,4-6H2,1-3H3
InChI key:YDBPZCVWPFMBDH-UHFFFAOYSA-N
SMILES:CC(C)(C)OC(=O)N1CCCC1C=O
Synonyms:
  • 2-Formylpyrrolidine-1-carboxylicacid tert-butyl ester
  • N-(Carbo-tert-butoxy)-2-pyrrolidinecarboxaldehyde
  • N-tert-Butoxycarbonylpyrrole-2-carboxaldehyde
  • 1-Boc-2-Formylpyrrolidine
  • 1-Pyrrolidinecarboxylicacid, 2-formyl-, 1,1-dimethylethyl ester
  • 1-Boc-pyrrolidine-2-carbaldehyde
  • 1-Pyrrolidinecarboxylicacid, 2-formyl-, 1,1-dimethylethyl es...
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