CAS 1255099-06-9

N-Benzyl-2-[6-(2-chloroacetylamino)-benzothiazol-2-ylsulfanyl]-acetamide

Description:

N-Benzyl-2-[6-(2-chloroacetylamino)-benzothiazol-2-ylsulfanyl]-acetamide is a synthetic organic compound characterized by its complex structure, which includes a benzyl group, a benzothiazole moiety, and an acetamide functional group. The presence of a chloroacetylamino group suggests potential reactivity, particularly in nucleophilic substitution reactions. This compound may exhibit biological activity due to its structural features, which could interact with various biological targets. The benzothiazole ring is known for its pharmacological properties, including antimicrobial and anticancer activities. Additionally, the sulfanyl group may contribute to the compound's reactivity and solubility in organic solvents. The molecular weight and specific physical properties, such as melting point and solubility, would depend on the precise arrangement of atoms and functional groups. Overall, N-Benzyl-2-[6-(2-chloroacetylamino)-benzothiazol-2-ylsulfanyl]-acetamide represents a class of compounds that may be of interest in medicinal chemistry and drug development.

Formula: C₁₈H₁₆ClN₃O₂S₂

Synonyms:

• N-Benzyl-2-[6-(2-chloroacetylamino)-benzothiazol-2-ylsulfanyl]-acetamide
• SKLB163
• SKLB 163
• SKLB-163

SKLB-163

CAS: 1255099-06-9

SKLB-163

Purity: ≥98%

Molecular weight: 405.92g/mol

Ref: 54-BUP12311

SKLB-163

CAS: 1255099-06-9

SKLB-163 acts by downregulating RhoGDI, activating JNK-1 signaling pathway and caspase-3, and reducing phosphorylated Akt and p44/42 MAPK.

Formula: C₁₈H₁₆ClN₃O₂S₂

Purity: 99.23%

Color and Shape: Solid

Molecular weight: 405.92

Ref: TM-T26193