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CAS 862273-27-6

:

Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, methyl ester, (1R,2S)-, 4-methylbenzenesulfonate (1:1)

Description:
Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, methyl ester, (1R,2S)-, 4-methylbenzenesulfonate (1:1) is a complex organic compound characterized by its cyclopropane ring structure, which contributes to its unique reactivity and strain. The presence of a carboxylic acid moiety indicates potential acidity and reactivity in various chemical reactions, while the methyl ester group suggests it can undergo hydrolysis to yield the corresponding acid. The (1R,2S) stereochemistry implies specific spatial arrangements of substituents, which can influence the compound's biological activity and interactions. The 4-methylbenzenesulfonate component serves as a counterion, enhancing solubility and stability in various solvents. This compound may exhibit interesting pharmacological properties due to its structural features, making it a subject of interest in medicinal chemistry. Its CAS number, 862273-27-6, allows for precise identification in chemical databases, facilitating research and application in various fields, including drug development and synthetic chemistry. Overall, this compound's unique structure and functional groups contribute to its potential utility in scientific research.
Formula:C7H11NO2·C7H8O3S
InChI:InChI=1S/C7H11NO2.C7H8O3S/c1-3-5-4-7(5,8)6(9)10-2;1-6-2-4-7(5-3-6)11(8,9)10/h3,5H,1,4,8H2,2H3;2-5H,1H3,(H,8,9,10)/t5-,7-;/m1./s1
InChI key:InChIKey=IUHJYIOSAPJUMG-HCSZTWNASA-N
SMILES:C(OC)(=O)[C@]1(N)[C@H](C=C)C1.S(=O)(=O)(O)C1=CC=C(C)C=C1
Synonyms:
  • (1R,2S)-methyl 1-Amino-2-ethenylcyclopropanecarboxylate 4-methylbenzenesulfonate
  • Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, methyl ester, (1R,2S)-, 4-methylbenzenesulfonate
  • cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, methyl ester, (1R,2S)-, 4-methylbenzenesulfonate (1:1)
  • methyl (1R,2S)-1-amino-2-ethenylcyclopropanecarboxylate 4-methylbenzenesulfonate (1:1)
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