89331-51-1 Usage
Molecular structure
The compound has a hydroxypropanol group and two amine groups attached to an ether and alkene linker.
Aromatic character
The compound features substituents with methoxy and dimethylamino groups on phenyl rings, giving it aromatic character.
Potential interactions with biological targets
The presence of methoxy and dimethylamino groups on phenyl rings suggests potential interactions with biological targets.
Hydroxypropanol moiety
The presence of the hydroxypropanol moiety indicates potential pharmaceutical applications or interactions with biological systems.
Unique properties and applications
The compound's complex structure suggests it may have unique properties and applications within the fields of medicinal chemistry, pharmacology, or material science.
Molecular weight
404.52 g/mol
Appearance
The compound is likely to be a solid or a viscous liquid, although the exact physical state is not specified in the material provided.
Solubility
The compound is likely to be soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO), although the exact solubility profile is not specified in the material provided.
Stability
The stability of the compound under various conditions (e.g., temperature, pH, light exposure) is not specified in the material provided. Further research would be needed to determine its stability profile.
Check Digit Verification of cas no
The CAS Registry Mumber 89331-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,3 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89331-51:
(7*8)+(6*9)+(5*3)+(4*3)+(3*1)+(2*5)+(1*1)=151
151 % 10 = 1
So 89331-51-1 is a valid CAS Registry Number.
89331-51-1Relevant articles and documents
Synthesis of β-blocking oximes. Influence of terminal amine on β-selectivity
Amlaiky,Leclerc,Decker,Schwartz
, p. 437 - 439 (2007/10/02)
Three series of oximinopropanolamine derivatives in which the terminal nitrogen has been substituted by various arylalkyl groups were synthesized. The beta-adrenergic blocking activity of the 21 compounds was determined in vitro on the guinea-pig. The structure-activity relationship is discussed.