IUPAC Name: Propyl 2-[4-[2-(diethylamino)-2-oxoethoxy]-3-methoxyphenyl]acetate
Synonyms of Propanidide (CAS NO.1421-14-3) : [3-Methoxy-4-[(N,N-diethylcarbamido)methoxy]phenyl]acetic Acid n-Propyl Ester ; [4-[(Diethylcarbamoyl)methoxy]-3-methoxyphenyl]acetic Acid Propyl Ester ; 4-[2-(Diethylamino)-2-oxoethoxy]-3-methoxybenzeneacetic Acid Propyl Ester ; Benzeneacetic acid, 4-(2-(diethylamino)-2-oxoethoxy)-3-methoxy-, propyl ester ; Propyl [4-[(Diethylcarbamoyl)methoxy]-3-methoxyphenyl]acetate ; Propyl {4-[2-(diethylamino)-2-oxoethoxy]-3-methoxyphenyl}acetate
InChI:InChI=1/C18H27NO5/c1-5-10-23-18(21)12-14-8-9-15(16(11-14)22-4)24-13-17(20)19(6-2)7-3/h8-9,11H,5-7,10,12-13H2,1-4H3
CAS NO:1421-14-3
Molecular Formula:C18H27NO5
Molecular Weight :337.4107
Molecular Structure :
EINECS: 215-822-7
Index of Refraction: 1.503
Surface Tension: 38.1 dyne/cm
Density: 1.087 g/cm3
Flash Point: 231.8 °C
Enthalpy of Vaporization: 72.02 kJ/mol
Boiling Point: 459.7 °C at 760 mmHg
Vapour Pressure: 1.24E-08 mmHg at 25°C
Propanidide (CAS NO.1421-14-3) is ultrashort intravenous anesthetics.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
cat | LD50 | intravenous | 80mg/kg (80mg/kg) | Acta Anaesthesiologica Scandinavica, Supplementum. Vol. 17, Pg. 21, 1965. | |
dog | LD50 | intravenous | 80mg/kg (80mg/kg) | Acta Anaesthesiologica Scandinavica, Supplementum. Vol. 17, Pg. 21, 1965. | |
human | TDLo | intravenous | 5mg/kg (5mg/kg) | BEHAVIORAL: GENERAL ANESTHETIC | British Journal of Anesthesia. Vol. 45, Pg. 1097, 1973. |
mouse | LD50 | intravenous | 113mg/kg (113mg/kg) | Oyo Yakuri. Pharmacometrics. Vol. 19, Pg. 845, 1980. | |
rabbit | LD50 | intravenous | 75mg/kg (75mg/kg) | Acta Anaesthesiologica Scandinavica, Supplementum. Vol. 17, Pg. 21, 1965. | |
rat | LD50 | intravenous | 81mg/kg (81mg/kg) | Acta Anaesthesiologica Scandinavica, Supplementum. Vol. 17, Pg. 21, 1965. | |
rat | LD50 | oral | > 10gm/kg (10000mg/kg) | Toxicology and Applied Pharmacology. Vol. 18, Pg. 185, 1971. |
Poison by intravenous route. Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive effects. Human systemic effects by intravenous route: general anesthesia. When Propanidide (CAS NO.1421-14-3) is heated to decomposition, it emits toxic fumes of NOx.
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