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5442-90-0

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5442-90-0 Usage

Chemical compound

2-[2-(morpholin-4-yl)-2-oxoethyl]-1H-isoindole-1,3(2H)-dione

Contains a morpholine ring

Heterocyclic organic compound used in pharmaceutical and chemical production

Contains an isoindole-1,3-dione ring

Important building block in organic synthesis

Potential applications in pharmaceutical industry

Possible precursor for drug synthesis

Complex structure

Requires extensive study and research to understand properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 5442-90-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5442-90:
(6*5)+(5*4)+(4*4)+(3*2)+(2*9)+(1*0)=90
90 % 10 = 0
So 5442-90-0 is a valid CAS Registry Number.

5442-90-0Relevant articles and documents

Synthesis and anticonvulsant properties of new acetamide derivatives of phthalimide, and its saturated cyclohexane and norbornene analogs

Kamiński, Krzysztof,Obniska, Jolanta,Wiklik, Beata,Atamanyuk, Dmytro

experimental part, p. 4634 - 4641 (2011/11/04)

The synthesis and anticonvulsant properties of new piperazine or morpholine acetamides derived from 2-(1,3-dioxoisoindolin-2-yl)-, 2-(1,3-dioxo-3a,4,5,6,7, 7a-hexahydroisoindol-2-yl-) and (3,5-dioxo-4-azatricyclo[5.2.1.0 2,6]dec-8-en-4-yl)-acetic acid were described. Initial anticonvulsant screening was performed using maximal electroshock (MES) and subcutaneous pentylenetetrazole (scPTZ) seizures tests. The neurotoxicity was determined applying the minimal motor impairment rotarod test. The in vivo results revealed that numerous compounds were effective in the MES screen. The most active was 2-{2-[4-(4-fluorophenyl)piperazin-1-yl]-2-oxoethyl}isoindoline-1,3-dione (12) that revealed protection in the electrically induced seizures at a dose of 30 mg/kg and 100 mg/kg 0.5 h and 4 h after i.p. administration in mice respectively. This molecule given orally in rats at a dose of 30 mg/kg was more potent than reference anticonvulsant - phenytoin.

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