(S)-2-(3'-Butenyl) Glycine, with the CAS number 90989-12-1, is an amino acid derivative characterized by its unique structure that includes a butenyl side chain attached to the glycine backbone. This compound is a chiral molecule, meaning it exists in two enantiomeric forms, with the (S) configuration being the biologically active form. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the butenyl group introduces unsaturation, which can influence its reactivity and interactions in biological systems. This compound may exhibit properties such as being a potential precursor in the synthesis of various bioactive molecules or serving as a building block in peptide synthesis. Its solubility in water and organic solvents can vary, affecting its applications in biochemical research and industrial processes. Overall, (S)-2-(3'-Butenyl) Glycine is of interest in fields such as medicinal chemistry and biochemistry due to its structural features and potential biological activities.

(S)-2-(3'-Butenyl) Glycine

90989-12-1: (S)-2-(3'-Butenyl) Glycine, with the CAS number 90989-12-1, is an amino acid derivative characterized by its unique structure that includes a butenyl side chain attached to the glycine backbone. This compound is a chiral molecule, meaning it exists in two enantiomeric forms, with the (S) configuration being the biologically active form. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the butenyl group introduces unsaturation, which can influence its reactivity and interactions in biological systems. This compound may exhibit properties such as being a potential precursor in the synthesis of various bioactive molecules or serving as a building block in peptide synthesis. Its solubility in water and organic solvents can vary, affecting its applications in biochemical research and industrial processes. Overall, (S)-2-(3'-Butenyl) Glycine is of interest in fields such as medicinal chemistry and biochemistry due to its structural features and potential biological activities.

CAS 90989-12-1

(S)-2-(3'-Butenyl) Glycine

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(S)-2-Aminohex-5-enoic acid

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