Cas 89331-61-3,1-(4-Dimethylamino-phenyl)-ethanone O-[2-hydroxy-3-(1-methyl-3-phenyl-propylamino)-propyl]-oxime; compound with (Z)-but-2-enedioic acid

89331-61-3

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Basic information

Product Name: 1-(4-Dimethylamino-phenyl)-ethanone O-[2-hydroxy-3-(1-methyl-3-phenyl-propylamino)-propyl]-oxime; compound with (Z)-but-2-enedioic acid
Synonyms:
CAS NO:89331-61-3
Molecular Formula:
Molecular Weight: 499.607
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(4-Dimethylamino-phenyl)-ethanone O-[2-hydroxy-3-(1-methyl-3-phenyl-propylamino)-propyl]-oxime; compound with (Z)-but-2-enedioic acid(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-Dimethylamino-phenyl)-ethanone O-[2-hydroxy-3-(1-methyl-3-phenyl-propylamino)-propyl]-oxime; compound with (Z)-but-2-enedioic acid(89331-61-3)
EPA Substance Registry System: 1-(4-Dimethylamino-phenyl)-ethanone O-[2-hydroxy-3-(1-methyl-3-phenyl-propylamino)-propyl]-oxime; compound with (Z)-but-2-enedioic acid(89331-61-3)

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: 89331-61-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89331-61-3 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, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89331-61:
(7*8)+(6*9)+(5*3)+(4*3)+(3*1)+(2*6)+(1*1)=153
153 % 10 = 3
So 89331-61-3 is a valid CAS Registry Number.

89331-61-3Upstream product

22374-89-6 (RS)-1-methyl-3-phenylpropylamine

89331-61-3Downstream Products

89331-61-3Relevant academic research and scientific papers

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.

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