CAS 765962-70-7

Ethyl 1-(chlorosulfonyl)-3-piperidinecarboxylate

Description:

Ethyl 1-(chlorosulfonyl)-3-piperidinecarboxylate is a chemical compound characterized by its unique functional groups and structure. It features a piperidine ring, which is a six-membered nitrogen-containing heterocycle, contributing to its basicity and potential for nucleophilic reactions. The presence of a chlorosulfonyl group (-SO2Cl) enhances its reactivity, making it a useful intermediate in organic synthesis, particularly in the formation of sulfonamide derivatives. The ethyl ester group (-COOEt) provides solubility in organic solvents and can be hydrolyzed to yield the corresponding carboxylic acid. This compound is typically handled with care due to the presence of the chlorosulfonyl moiety, which can be reactive and potentially hazardous. Its applications may include medicinal chemistry, where it could serve as a building block for pharmaceuticals, or in agrochemical synthesis. Overall, Ethyl 1-(chlorosulfonyl)-3-piperidinecarboxylate is notable for its reactivity and versatility in synthetic organic chemistry.

Formula: C₈H₁₄ClNO₄S

InChI: InChI=1S/C8H14ClNO4S/c1-2-14-8(11)7-4-3-5-10(6-7)15(9,12)13/h7H,2-6H2,1H3

InChI key: InChIKey=AYLNINMKMQOFAN-UHFFFAOYSA-N

SMILES: C(OCC)(=O)C1CN(S(Cl)(=O)=O)CCC1

Synonyms:

• 3-Piperidinecarboxylic acid, 1-(chlorosulfonyl)-, ethyl ester
• Ethyl 1-(chlorosulfonyl)-3-piperidinecarboxylate
• ethyl 1-(chlorosulfonyl)piperidine-3-carboxylate(SALTDATA: FREE)