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CAS 1329035-82-6

:

Trans-(1S,4S)-4-Boc-aMino-2-Cyclopentene-1-carboxylic acid

Description:
Trans-(1S,4S)-4-Boc-amino-2-cyclopentene-1-carboxylic acid is a chemical compound characterized by its unique bicyclic structure, which includes a cyclopentene ring. The "Boc" (tert-butyloxycarbonyl) group is a protective group commonly used in organic synthesis to shield amines during reactions. This compound features a carboxylic acid functional group, which contributes to its acidity and reactivity. The stereochemistry indicated by the (1S,4S) configuration suggests specific spatial arrangements of the substituents around the chiral centers, which can significantly influence the compound's biological activity and interactions. The trans configuration denotes that the substituents on the cyclopentene ring are positioned opposite each other, affecting the compound's overall shape and properties. This compound may be of interest in medicinal chemistry and peptide synthesis due to its structural features, which can mimic natural amino acids or serve as building blocks for more complex molecules. Its CAS number, 1329035-82-6, allows for precise identification in chemical databases and literature.
Formula:C11H17NO4
Synonyms:
  • (1S,4S)-4-((tert-Butoxycarbonyl)amino)cyclopent-2-enecarboxylic acid
  • (1S,4S)-4-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-cyclopentene-1-carboxylic acid
  • 2-Cyclopentene-1-carboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, (1S,4S)-
  • (1S,4S)-4-((tert-butoxycarbonyl)amino)cyclopent-2-ene-1-carboxylic acid
  • Trans-(1S,4S)-4-Boc-aMino-2-Cyclopentene-1-carboxylic acid
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