Cas 1583305-50-3,2-(4-dimethylamino-phenyl)-5-methoxy-1-oxy-indol-3-one, hydrochloride

1583305-50-3

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Basic information

Product Name: 2-(4-dimethylamino-phenyl)-5-methoxy-1-oxy-indol-3-one, hydrochloride
Synonyms: 2-(4-dimethylamino-phenyl)-5-methoxy-1-oxy-indol-3-one, hydrochloride
CAS NO:1583305-50-3
Molecular Formula:
Molecular Weight: 332.787
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: 2-(4-dimethylamino-phenyl)-5-methoxy-1-oxy-indol-3-one, hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-dimethylamino-phenyl)-5-methoxy-1-oxy-indol-3-one, hydrochloride(1583305-50-3)
EPA Substance Registry System: 2-(4-dimethylamino-phenyl)-5-methoxy-1-oxy-indol-3-one, hydrochloride(1583305-50-3)

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: 1583305-50-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1583305-50-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,3,3,0 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1583305-50:
(9*1)+(8*5)+(7*8)+(6*3)+(5*3)+(4*0)+(3*5)+(2*5)+(1*0)=163
163 % 10 = 3
So 1583305-50-3 is a valid CAS Registry Number.

1583305-50-3Upstream product

1133205-30-7 2-(4-aminophenyl)-5-methoxy-1-oxyindol-3-one

1583305-50-3Downstream Products

1583305-50-3Relevant academic research and scientific papers

Amino derivatives of indolone-N-oxide: Preparation and antiplasmodial properties

Najahi, Ennaji,Rakotoarivelo, Nambinina V.,Valentin, Alexis,Nepveu, Fran?oise

, p. 369 - 375 (2014)

There is an urgent need for new antimalarial drugs with novel mechanisms of action on novel targets. Indolone-N-oxides (INODs) display antimalarial properties in vitro and in vivo, but identified leads such as 6-(4-chloro-phenyl)-5-oxy-[1,3]dioxolo[4,5-f]

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