864447-25-6

Basic information

• Product Name: C₈₄H₈₄Cl₂N₈O₂₉
• CAS NO: 864447-25-6
• Molecular Weight: 1740.53
• Mol File: 864447-25-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₈₄H₈₄Cl₂N₈O₂₉(CAS DataBase Reference)
• NIST Chemistry Reference: C₈₄H₈₄Cl₂N₈O₂₉(864447-25-6)
• EPA Substance Registry System: C₈₄H₈₄Cl₂N₈O₂₉(864447-25-6)

Safety Data

• Hazardous Substances Data: 864447-25-6(Hazardous Substances Data)

Upstream product

• 5736-94-7 4-(hexyloxy)benzaldehyde 
• 118693-63-3 N'-deacyl A₄₀₉₂₆ 

Downstream Products

• 864447-36-9 C₉₄H₁₀₈Cl₂N₁₂O₂₇ 

Relevant articles and documents

Synthesis and antibacterial activity of alkyl derivatives of the glycopeptide antibiotic A40926 and their amides

New derivatives of the glycopeptide antibiotic A40926 were synthesized and evaluated for antimicrobial activity against VRE. Deacylated A40926 was obtained by microbial transformation of the parent antibiotic with the use of Actinoplanes teichomyceticus ATCC 31121. Regioselective synthesis of alkylated derivatives of Deacyl A40926 was carried out using lipophilic aliphatic and aromatic halides or aldehydes. Further modification of the two carboxylic acids was performed to increase antibiotic activity. Poor antimicrobial activity was observed for the derivatives obtained by lipophilic mono- or dialkylation of the amino groups present on the molecule, while simultaneous condensation of both carboxylic groups, in hydrophobic derivatives, with dibasic amines led to a strong increase in antibiotic activity.