- Soterenol
- Soterenol hydrochloride
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| Name |
Soterenol |
EINECS | N/A |
| CAS No. | 13642-52-9 | Density | 1.321g/cm3 |
| PSA | 107.04000 | LogP | 2.33980 |
| Solubility | N/A | Melting Point |
N/A |
| Formula | C12H20N2O4S | Boiling Point | 477°Cat760mmHg |
| Molecular Weight | 288.368 | Flash Point | 242.3°C |
| Transport Information | N/A | Appearance | N/A |
| Safety | Poison by ingestion, subcutaneous, intravenous and intraperitoneal routes. When heated to decomposition it emits very toxic fumes of SOx and NOx. See also SOTERENOL HYDROCHLORIDE. | Risk Codes | N/A |
| Molecular Structure |
|
Hazard Symbols | N/A |
| Synonyms |
Soterenol |
Soterenol Chemical Properties
IUPAC Name: N-[2-Hydroxy-5-[1-hydroxy-2-(propan-2-ylamino)ethyl]phenyl]methanesulfonamide
Molecular Formula: C12H20N2O4S
Molecular Weight: 288.40
Freely Rotating Bonds: 7
Polar Surface Area: 67.46 Å2
Index of Refraction: 1.59
Molar Refractivity: 73.66 cm3
Molar Volume: 218.1 cm3
Polarizability: 29.2 ×10-24 cm3
Surface Tension: 57.6 dyne/cm
Density: 1.321 g/cm3
Flash Point: 242.3 °C
Enthalpy of Vaporization: 78.04 kJ/mol
Boiling Point: 477 °C at 760 mmHg
Vapour Pressure: 6.58E-10 mmHg at 25°C
The Cas Register Number of Soterenol is 13642-52-9.The chemical synonyms of Soterenol (CAS NO.13642-52-9) are 2'-Hydroxy-5'-[1-hydroxy-2-(isopropylamino)eth yl]methanesulfonanilide ; Methanesulfonamide, N-(2-hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)ethyl)phenyl)- ; N-[2-Hydroxy-5-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]methanesulfonamide ; N-{2-Hydroxy-5-[1-hydroxy-2-(isopropylamino)ethyl]phenyl}methanesulfonamide and 2'-Hydroxy-5'-(1-hydroxy-2-isopropylaminoethyl)methansulfonilid .The molecular structure of Soterenol (CAS NO.13642-52-9) is
.
Soterenol Uses
Soterenol (CAS NO.13642-52-9) is used as organic intermediate.
Soterenol Toxicity Data With Reference
| 1. | orl-mus LD50:1140 mg/kg | JPETAB Journal of Pharmacology and Experimental Therapeutics. 164 (1968),290. | ||
| 2. | ipr-mus LD50:335 mg/kg | JPETAB Journal of Pharmacology and Experimental Therapeutics. 164 (1968),290. | ||
| 3. | ivn-mus LD50:47 mg/kg | JPETAB Journal of Pharmacology and Experimental Therapeutics. 164 (1968),290. | ||
| 4. | ivn-dog LD50:1 mg/kg | JPETAB Journal of Pharmacology and Experimental Therapeutics. 164 (1968),290. | ||
| 5. | orl-gpg LD50:41 mg/kg | JPETAB Journal of Pharmacology and Experimental Therapeutics. 164 (1968),290. | ||
| 6. | scu-gpg LD50:14 mg/kg | JPETAB Journal of Pharmacology and Experimental Therapeutics. 164 (1968),290. |
Soterenol Safety Profile
Poison by ingestion, subcutaneous, intravenous and intraperitoneal routes. When heated to decomposition it emits very toxic fumes of SOx and NOx. See also SOTERENOL HYDROCHLORIDE.
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