CAS 2787-09-9

Acetamide,2,2-dichloro-N-[(1R,2R)-2-hydroxy-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl]-,rel-

Description:

Acetamide, 2,2-dichloro-N-[(1R,2R)-2-hydroxy-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl]-, rel- is a chemical compound characterized by its complex structure, which includes an acetamide functional group and multiple substituents that contribute to its unique properties. The presence of dichloro groups indicates that it has two chlorine atoms attached to the carbon backbone, which can influence its reactivity and solubility. The compound also features a hydroxy group and a nitrophenyl moiety, which can enhance its biological activity and potential applications in pharmaceuticals or agrochemicals. Its stereochemistry, indicated by the (1R,2R) configuration, suggests specific spatial arrangements that may affect its interactions with biological targets. The CAS number 2787-09-9 allows for precise identification and retrieval of information regarding this compound in chemical databases. Overall, this substance may exhibit interesting chemical behavior and potential utility in various fields, including medicinal chemistry and materials science.

Formula: C₁₁H₁₂Cl₂N₂O₅

Synonyms:

• Acetamide,2,2-dichloro-N-[2-hydroxy-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl]-, (R*,R*)-(?à)-
• Acetamide, 2,2-dichloro-N-[b-hydroxy-a-(hydroxymethyl)-p-nitrophenethyl]-,DL-threo- (8CI)
• (?à)-Chloramphenicol
• Acetamide,2,2-dichloro-N-[2-hydroxy-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl]-, (R*,R*)-
• DL-Chloramphenicol
• DL-trans-1-p-Nitrophenyl-2-dichloroacetylamino-1,3-propanediol
• Synthomycin
• Syntomycin

DL-Chloramphenicol

Controlled Product

CAS: 2787-09-9

Formula: C₁₁H₁₂Cl₂N₂O₅

Color and Shape: Neat

Molecular weight: 323.129

Ref: TR-C584520

DL-chloramphenicol

CAS: 2787-09-9

DL-chloramphenicol is a broad-spectrum antibiotic, which is a synthetic compound derived from natural chloramphenicol originally isolated from the bacterium Streptomyces venezuelae. This compound exerts its effects by inhibiting bacterial protein synthesis. It binds to the 50S subunit of the bacterial ribosome, preventing peptide bond formation and consequently halting the growth of susceptible bacteria. The optical isomer, DL-chloramphenicol, contains equal parts of both D- and L- isomers, with the L-form being responsible for its antibiotic activity.

Formula: C₁₁H₁₂Cl₂N₂O₅

Purity: Min. 95%

Molecular weight: 323.13 g/mol

Ref: 3D-CAA78709