6-[O-3-AcetaMido-3-deoxy-α-D-glucopyranosyl-4-O-[6-acetaMido-6-deoxy-α-D-glucopyranosyl]-N,N'-diacetyl-2-deoxy-L-streptaMine

Base Information

• Chemical Name: 6-[O-3-AcetaMido-3-deoxy-α-D-glucopyranosyl-4-O-[6-acetaMido-6-deoxy-α-D-glucopyranosyl]-N,N'-diacetyl-2-deoxy-L-streptaMine
• CAS No.: 20399-23-9
• Molecular Formula: C₂₆H₄₄N₄O₁₅
• Molecular Weight: 652.653
• Mol file: 20399-23-9.mol

Synonyms:4-[O-3-AcetaMido-3-deoxy-α-D-glucopyranosyl-6-O-[6-acetaMido-6-deoxy-α-D-glucopyranosyl]-N,N'-diacetyl-2-deoxy-L-streptaMine;6-[O-3-AcetaMido-3-deoxy-α-D-glucopyranosyl-4-O-[6-acetaMido-6-deoxy-α-D-glucopyranosyl]-N,N'-diacetyl-2-deoxy-L-streptaMine;Tetra-N-acetyl KanaMycin A

Chemical Property of 6-[O-3-AcetaMido-3-deoxy-α-D-glucopyranosyl-4-O-[6-acetaMido-6-deoxy-α-D-glucopyranosyl]-N,N'-diacetyl-2-deoxy-L-streptaMine

Chemical Property:

• PSA: 308.89000
• LogP: -3.22060
• Storage Temp.: Refrigerator
• Solubility.: Methanol, Water

Purity/Quality:

99% ^*data from raw suppliers

Tetra-N-acetyl Kanamycin A ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Protected Kanamycin A (K137500). Antibiotic complex produced by Streptomyces kanamyceticus Okami & Umezawa from Japanese soil. Comprised of three components, kanamycin A, the major component, and kana mycins B and C, two minor congeners. Antibacterial. Protected Kanamycin A (K137500). Antibiotic complex produced by Streptomyces kanamyceticus Okami & Umezawa from Japanese soil. Comprised of three components, kanamycin A, the major component, and kanamycins B and C, two minor congeners. Antibacterial.

Technology Process of 6-[O-3-AcetaMido-3-deoxy-α-D-glucopyranosyl-4-O-[6-acetaMido-6-deoxy-α-D-glucopyranosyl]-N,N'-diacetyl-2-deoxy-L-streptaMine

There total 1 articles about 6-[O-3-AcetaMido-3-deoxy-α-D-glucopyranosyl-4-O-[6-acetaMido-6-deoxy-α-D-glucopyranosyl]-N,N'-diacetyl-2-deoxy-L-streptaMine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ tetra-N-acetyl-kanamycin A (20399-23-9,22860-90-8,37091-21-7)

Guidance literature:

With methanol; acetic anhydride;

DOI:10.1021/ja01536a058

Reference yield:

tetra-N-acetyl-kanamycin A (20399-23-9,22860-90-8,37091-21-7) → Tetra-N-acetyl-hepta-O-methyl-kanamycin-A (884594-78-9)

Guidance literature:

With tetrachloromethane; sodium hydroxide; dimethyl sulfate;

DOI:10.1246/bcsj.32.81

Downstream raw materials:

Tetra-N-acetyl-hepta-O-methyl-kanamycin-A

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