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3-(4-methoxy-phenyl)-1,3-diaza-spiro[4.5]decane-2,4-dione is a complex organic compound with a molecular formula of C14H18N2O3. It is a derivative of 1,3-diaza-spiro[4.5]decane-2,4-dione, featuring a 4-methoxy-phenyl group attached to the nitrogen atom at the 3-position. 3-(4-methoxy-phenyl)-1,3-diaza-spiro[4.5]decane-2,4-dione is characterized by its unique spirocycle structure, which consists of a seven-membered ring fused to a five-membered ring, with two nitrogen atoms incorporated into the structure. The presence of the 4-methoxy-phenyl group imparts additional electronic and steric properties to the molecule, which can influence its reactivity, solubility, and potential applications in various chemical and pharmaceutical contexts.

894-23-5

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894-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 894-23-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 894-23:
(5*8)+(4*9)+(3*4)+(2*2)+(1*3)=95
95 % 10 = 5
So 894-23-5 is a valid CAS Registry Number.

894-23-5Relevant academic research and scientific papers

GLYT1 TRANSPORTER INHIBITORS AND USES THEREOF IN TREATMENT OF NEUROLOGICAL AND NEUROPSYCHIATRIC DISORDERS

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Page/Page column 35-36, (2008/12/07)

Compounds of Formula (I) or a salt thereof are provided: wherein R6, R7, R8, R21, X, Ar, and m are as defined in the description. Uses of the compounds as medicaments, and in the manufacture of medicament for treating neurological and neuropsychiatric disorders, in particular psychoses, dementia or attention deficit disorder are also disclosed. The invention further discloses pharmaceutical compositions and combinations comprising the compounds.

Synthesis, selective aldose reductase inhibitory profile and antihyperglycaemic potential of certain parabanic acid derivatives

Nabil Aboul-Enein,El-Azzounya,Maklad,Attia,Wiese

, p. 329 - 350 (2007/10/03)

Synthesis and aldose reductase inhibitory profile of certain parabanic acid derivatives 1a-p is described. Also, the antihyperglycaemic potential of these compounds was studied. The most active inhibitors in this series were compounds 1 g, 1p, and 1o which showed inhibitory activity, 36.6, 90 and 91% respectively, at concentration 1 × 10-4. Their IC50 were 2 × 10-6, 7.5 × 10-8 and 5 × 10-8, respectively. Compound 1o exhibited pronounced antihyperglycaemic effect.

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