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CAS No.: | 37415-62-6 |
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Name: | 4-Hexenoic acid,6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-,sodium salt (1:1), (4E)- |
Molecular Structure: | |
Formula: | C17H19O6.Na |
Molecular Weight: | 342.35 |
Synonyms: | 4-Hexenoicacid, 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-,monosodium salt, (4E)- (9CI);4-Hexenoic acid,6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-,monosodium salt, (E)-;EC-MPS;ERL 080;ERL 080A;Mycophenolate sodium;Mycophenolic acid monosodium salt;Mycophenolic monosodium salt;Myfortic; |
Density: | 1.29 g/cm3 |
Boiling Point: | 611.6 °C at 760 mmHg |
Flash Point: | 225.8 °C |
PSA: | 93.06000 |
LogP: | 2.73320 |
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Molecular Structure:
Molecular Formula: C17H19NaO6
Molecular Weight: 342.3189
IUPAC Name: SAodium (E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1H-2-benzofuran-5-yl)-4-methylhex-4-enoate
Synonyms of Sodium mycophenolate (CAS NO.37415-62-6): 4-Hexenoic acid, 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-, monosodium salt, (4E)- ; ERL 080 ; ERL 080A ; Mycophenolate sodium ; Mycophenolic acid monosodium salt ; Mycophenolic acid, sodium salt ; Myfortic ; NSC 116072 ; Sodium 4(E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydroisobenzofuran-5-yl)-4-methylhex-4-enoate ; UNII-WX877SQI1G ; 4-Hexenoic acid, 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-, monosodium salt, (E)- (9CI) ; 4-Hexenoic acid, 6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-5-phthalanyl)-4-methyl-, sodium salt
CAS NO: 37415-62-6
Classification Code: Immunosuppressant ; Mutation data ; Natural Product ; Transplantation [immunosuppressant]
Flash Point: 225.8 °C
Enthalpy of Vaporization: 95.48 kJ/mol
Boiling Point: 611.6 °C at 760 mmHg
Vapour Pressure: 8.18E-16 mmHg at 25°C
Sodium mycophenolate (CAS NO.37415-62-6) is a derivative of mycophenolic acid, with anti-virus, anti-bacterial, anti-fungal, anti-cancer, immune suppression and other benefits.
Sodium mycophenolate (CAS NO.37415-62-6) can be derived from Mycophenolic acid .
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
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mouse | LD | subcutaneous | > 400mg/kg (400mg/kg) | Lancet. Vol. 250, Pg. 46, 1946. | |
mouse | LD50 | intraperitoneal | 568mg/kg (568mg/kg) | Antimicrobial Agents and Chemotherapy Vol. -, Pg. 229, 1968. | |
mouse | LD50 | oral | 1176mg/kg (1176mg/kg) | Antimicrobial Agents and Chemotherapy Vol. -, Pg. 229, 1968. | |
mouse | LDLo | intravenous | 400mg/kg (400mg/kg) | Lancet. Vol. 250, Pg. 46, 1946. |
Poison by intravenous route. Moderately toxic by ingestion and intraperitoneal routes. Mutation data reported. When heated to decomposition it emits toxic fumes of Na2O.