Cas 197909-67-4,1,6'-Di-HABA KanaMycin A

197909-67-4

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Basic information

Product Name: 1,6'-Di-HABA KanaMycin A
Synonyms: 1,6'-Di-HABA KanaMycin A;1,6'-Di-N-(L-4-aMino-2-hydroxybutyryl) KanaMycin A;O-3-AMino-3-deoxy-α-D-glucopyranosyl-(1→6)-O-[6-[[(2S)-4-aMino-2-hydroxy-1-oxobutyl]aMino]-6-deoxy-α-D-glucopyranosyl-(1→4)]-N1-[(2S)-4-aMino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptaMine
CAS NO:197909-67-4
Molecular Formula: C26H50N6O15
Molecular Weight: 686.7064
EINECS: N/A
Product Categories: Amines;Intermediates & Fine Chemicals;Oligosaccharides;Pharmaceuticals
Mol File: 197909-67-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 1131.0±65.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.59±0.1 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 12.92±0.70(Predicted)
CAS DataBase Reference: 1,6'-Di-HABA KanaMycin A(CAS DataBase Reference)
NIST Chemistry Reference: 1,6'-Di-HABA KanaMycin A(197909-67-4)
EPA Substance Registry System: 1,6'-Di-HABA KanaMycin A(197909-67-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 197909-67-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 197909-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,9,0 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 197909-67:
(8*1)+(7*9)+(6*7)+(5*9)+(4*0)+(3*9)+(2*6)+(1*7)=204
204 % 10 = 4
So 197909-67-4 is a valid CAS Registry Number.

197909-67-4Upstream product

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197909-67-4Relevant academic research and scientific papers

Synthesis and Biological Activity of Mono- and Di-N-acylated Aminoglycosides

Chandrika, Nishad Thamban,Green, Keith D.,Houghton, Jacob L.,Garneau-Tsodikova, Sylvie

supporting information, p. 1134 - 1139 (2015/11/24)

Despite issues with oto/nephrotoxicity and bacterial resistance, aminoglycosides (AGs) remain an effective and widely used class of antibacterial agents. For decades now, efforts toward the development of novel AGs with potential to overcome some of these

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