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CAS No.: | 35483-50-2 |
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Name: | Viriditoxin |
Molecular Structure: | |
Formula: | C34H30 O14 |
Molecular Weight: | 482.56 |
Synonyms: | [8,8'-Bi-1H-naphtho[2,3-c]pyran]-3,3'-diaceticacid, 3,3',4,4'-tetrahydro-9,9',10,10'-tetrahydroxy-7,7'-dimethoxy-1,1'-dioxo-,dimethyl ester (9CI); 1H-Naphtho[2,3-c]pyran, bimol. deriv.;3,3'-di(Methylcarboxymethyl)-3,3',4,4'-tetrahydro-9,9',10,10'-tetrahydroxy-7,7'-dimethoxy-1,1'-dioxo-8,8'-bi-1H-naphtho[2,3-c]pyran;SC 28762; Viriditoxin; Viriditoxin (Aspergillus) |
Density: | 1.477g/cm3 |
Melting Point: | 243.5°C (rough estimate) |
Boiling Point: | 833.6°Cat760mmHg |
Flash Point: | 265.9°C |
Safety: | Poison by intramuscular and intraperitoneal routes. An experimental teratogen. When heated to decomposition it emits acrid smoke and irritating fumes. |
PSA: | 204.58000 |
LogP: | 3.78880 |
Chemistry informtion about Viriditoxin (CAS NO.35483-50-2) is:
IUPAC Name: Methyl 2-[8-[9,10-Dihydroxy-7-Methoxy-3-(2-Methoxy-2-Oxoethyl)-1-Oxo-3,4-Dihydrobenzo[G]Isochromen-8-Yl]-9,10-Dihydroxy-7-Methoxy-1-Oxo-3,4-Dihydrobenzo[G]Isochromen-3-Yl]Acetate
Synonyms: Viriditoxin ; 3,3',4,4'-Tetrahydro-9,9',10,10'-Tetrahydroxy-7,7'-Dimethoxy-1,1'-Dioxo-(8,8'-Bi-1h-Naphtho[2,3-C]Pyran)-3,3'-Diacetic Acid Dimethyl Ester ; 3,3',4,4'-Tetrahydro-9,9',10,10'-Tetrahydroxy-7,7'-Dimethoxy-1,1'-Dioxo-8,8'-Bi(1h-Naphtho[2,3-C]Pyran)-3,3'-Diacetic Acid Dimethyl ; 3,3',4,4'-Tetrahydro-9,9',10,10'-Tetrahydroxy-7,7'-Dimethoxy-1,1'-Dioxo-8,8'-Bi(1h-Naphtho[2,3-C]Pyran)-3,3'-Diacetic Acid Dimethyl Ester ; Sc-28762
MF: C34H30O14
MW: 662.593600 g/mol
Density: 1.477 g/cm3
Flash Point: 265.9 °C
Boiling Point: 833.6 °C at 760 mmHg
Vapour Pressure: 4.83E-29 mmHg at 25°C
Enthalpy of Vaporization: 125.31 kJ/mol
Following is the molecular structure of Viriditoxin (CAS NO.35483-50-2) is:
Safty information about Viriditoxin (CAS NO.35483-50-2) is:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 2800ug/kg (2.8mg/kg) | "CRC Handbook of Antibiotic Compounds," Vols.1- , Berdy, J., Boca Raton, FL, CRC Press, 1980Vol. 5, Pg. 408, 1981. |
Poison by intramuscular and intraperitoneal routes. An experimental teratogen. When heated to decomposition it emits acrid smoke and irritating fumes.