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IUPAC Name: 2-Amino-N-(1,5,6-trihydroxy-3-methyl-8-oxo-3,4,4a,5,6,7-hexahydroisochromen-4-yl)propanamide
Molecular Formula: C13H20N2O6
Molecular Weight: 300.31g/mol
Density: 1.45g/cm3
Flash Point: 311.9°C
Freely Rotating Bonds: 6
Polar Surface Area: 142.11 Å2
Index of Refraction: 1.607
Molar Refractivity: 71.32 cm3
Molar Volume: 206.3 cm3
Polarizability: 28.27 ×10-24cm3
Surface Tension: 71.1 dyne/cm
Enthalpy of Vaporization: 107.85 kJ/mol
Boiling Point: 637.2 °C at 760 mmHg
Vapour Pressure: 6.45E-19 mmHg at 25°C
The Cas Register Number of Actinobolin is 24397-89-5 .The chemical synonyms of Actinobolin (CAS No. 24397-89-5) are Propanamide, 2-amino-n-(3,4,4a,5,6,7-hexahydro-5,6, 8-trihydroxy-3-met hyl-1-oxo-1h-2-benzopyran-4-yl)- ; Actinobolin ; (3R)-4α-[[(s)-2-aminopropanoyl]amino]-3,4,4aβ,5,6,7-hexahydro-5β,6α,8-trihydroxy-3α-methyl-1h-2-benzopyran-1-one ; (S)-2-Amino-n-[(3r)-3,4,4aβ,5,6,7-hexahydro-5β,6α,8-trihydroxy-3α-methyl-1-oxo-1h-2-benzopyran-4α-yl]propanamide ; (S)-2-Amino-n-[(3r,4r,4ar,5r,6r)-3,4,4a,5,6,7-hexahydro-5,6,8-trihydroxy-3-methyl-1-oxo-1h-2-benzopyran-4-yl]propanamide ; (S)-N-[(3R)-3,4,4aβ,5,6,7-hexahydro-5β,6α,8-trihydroxy-3α-methylisocoumarin-4α-yl]-2-aminopropion .The molecular structure of Actinobolin (CAS No. 24397-89-5) is.
Actinobolin (CAS No. 24397-89-5) can be used in organic synthesis.
1. | pic-esc 240 mg/L | ZAPOAK Zeitschrift fuer Allgemeine Mikrobiologie. Morphologie, Physiologie, Genetik und Oekologie der Mikroorganismen. 8 (1968),139. | ||
2. | ipr-mus LD50:2844 mg/kg | NCISP* National Cancer Institute Screening Program Data Summary, Developmental Therapeutics Program, Bethesda, MD 20205 JAN86 . | ||
3. | scu-mus LD50:1828 mg/kg | NCISP* National Cancer Institute Screening Program Data Summary, Developmental Therapeutics Program, Bethesda, MD 20205 JAN86 . | ||
4. | ivn-mus LD50:6250 µg/kg | JANTAJ Journal of Antibiotics. 32 (1979),1069. | ||
5. | unr-mus LDLo:2000 mg/kg | 85ERAY Antibiotics: Origin, Nature, and Properties . 2 Korzyoski, T.,Z. Kowszyk-Gindifer, andW. Kurylowicz, eds.,Washington DC.: American Society for Microbiology(1978),1368. |
Poison by intravenous route. Moderately toxic by other routes. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. An antimicrobial agent and experimental cariostat.