Cyclohexanaminium (S)-2-azido-4-(methylthio)butanoate is a chemical compound characterized by its unique structural features, which include a cyclohexane ring and an azido functional group. The presence of the azido group (-N3) suggests potential reactivity, particularly in click chemistry applications, where it can participate in various coupling reactions. The methylthio group (-S-CH3) contributes to the compound's overall polarity and may influence its solubility in organic solvents. The butanoate moiety indicates that the compound is a derivative of butanoic acid, which can affect its biological activity and interactions. This compound may exhibit interesting pharmacological properties due to its structural complexity, making it a candidate for further research in medicinal chemistry. Additionally, the stereochemistry indicated by the (S) configuration suggests specific spatial arrangements that could impact its reactivity and interactions with biological targets. Overall, cyclohexanaminium (S)-2-azido-4-(methylthio)butanoate presents a fascinating subject for study in both synthetic and applied chemistry contexts.

cyclohexanaminium (S)-2-azido-4-(methylthio)butanoate

1217445-93-6: Cyclohexanaminium (S)-2-azido-4-(methylthio)butanoate is a chemical compound characterized by its unique structural features, which include a cyclohexane ring and an azido functional group. The presence of the azido group (-N3) suggests potential reactivity, particularly in click chemistry applications, where it can participate in various coupling reactions. The methylthio group (-S-CH3) contributes to the compound's overall polarity and may influence its solubility in organic solvents. The butanoate moiety indicates that the compound is a derivative of butanoic acid, which can affect its biological activity and interactions. This compound may exhibit interesting pharmacological properties due to its structural complexity, making it a candidate for further research in medicinal chemistry. Additionally, the stereochemistry indicated by the (S) configuration suggests specific spatial arrangements that could impact its reactivity and interactions with biological targets. Overall, cyclohexanaminium (S)-2-azido-4-(methylthio)butanoate presents a fascinating subject for study in both synthetic and applied chemistry contexts.

CAS 1217445-93-6

cyclohexanaminium (S)-2-azido-4-(methylthio)butanoate

Butanoic acid, 2-azido-4-(methylthio)-, compd. with cyclohexanamine (1:1), (2S)-

Ref: IN-DA0015P7

(S)-2-Azido-4-(methylthio)butanoic acid cyclohexylammonium salt

Ref: 7W-GM5240

L-azidomethionine CHA salt

Ref: 54-BICR402