13642-52-9
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Basic information
- Product Name: Soterenol
- Synonyms: Soterenol;2-(Methylsulfonylamino)-4-[1-hydroxy-2-(isopropylamino)ethyl]phenol;N-[2-Hydroxy-5-[1-hydroxy-2-(isopropylamino)ethyl]phenyl]methanesulfonamide;N-[2-Hydroxy-5-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]methanesulfonamide;Soternol
- CAS NO:13642-52-9
- Molecular Formula: C12H20N2O4S
- Molecular Weight: 288.40
- EINECS: N/A
- Product Categories: N/A
- Mol File: 13642-52-9.mol
- Article Data: 0
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 477°Cat760mmHg
- Flash Point: 242.3°C
- Appearance: /
- Density: 1.2631 (rough estimate)
- Vapor Pressure: 6.58E-10mmHg at 25°C
- Refractive Index: 1.6930 (estimate)
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 8.57±0.50(Predicted)
- CAS DataBase Reference: Soterenol(CAS DataBase Reference)
- NIST Chemistry Reference: Soterenol(13642-52-9)
- EPA Substance Registry System: Soterenol(13642-52-9)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 13642-52-9(Hazardous Substances Data)
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13642-52-9 Usage
Check Digit Verification of cas no
The CAS Registry Mumber 13642-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,4 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.Calculate Digit Verification of CAS Registry Number 13642-52:
(7*1)+(6*3)+(5*6)+(4*4)+(3*2)+(2*5)+(1*2)=89
89 % 10 = 9
So 13642-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H20N2O4S/c1-8(2)13-7-12(16)9-4-5-11(15)10(6-9)14-19(3,17)18/h4-6,8,12-16H,7H2,1-3H3
13642-52-9Upstream product
13642-52-9Downstream Products
13642-52-9Related news
Short communicationPotent α-adrenoceptor action of Soterenol (cas 13642-52-9) on vascular and other smooth muscle09/06/2019
Treatment with soterenol (0.3–300 μg/kg, i.v.) increased the mean arterial blood pressure and decreased heart rate in rabbits. Soterenol caused a dose-dependent contraction of rabbit aorta and portal vein, guinea-pig vas deferens and cat nictitating membrane which was inhibited by phentolamine...detailed
NoteApplication of Trihydroxyindole Reaction to Methanesulfonanilides: Fluorometric Analysis for Soterenol (cas 13642-52-9) and Mesuprine09/05/2019
Methanesulfonanilides, like soterenol and mesuprine, which are bioisosteric with adrenergic catecholamines, form fluorescent species when subjected to the trihydroxyindole reaction. Presumably, the fluorescence is due to adrenolutin‐like species formed from aminochrome intermediates. Fluorescen...detailed
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