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"2-(4-Benzyl-piperidin-1-yl)-6,7-dimethoxy-quinazolin-4-ylamine; hydrochloride" is a complex organic compound with the molecular formula C26H30ClN3O2. It is a derivative of quinazolin-4-ylamine, featuring a benzyl-piperidin-1-yl group at the 2-position, and two methoxy groups at the 6 and 7 positions. The hydrochloride salt form indicates that it is protonated, which can affect its solubility and stability in certain environments. 2-(4-Benzyl-piperidin-1-yl)-6,7-dimethoxy-quinazolin-4-ylamine; hydrochloride is of interest in medicinal chemistry, potentially for its interactions with biological targets due to its unique structure. It is important to note that the specific applications, pharmacological properties, and safety profile of 2-(4-Benzyl-piperidin-1-yl)-6,7-dimethoxy-quinazolin-4-ylamine; hydrochloride would require further detailed study and are not covered in this brief summary.

23673-00-9

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23673-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23673-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,7 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23673-00:
(7*2)+(6*3)+(5*6)+(4*7)+(3*3)+(2*0)+(1*0)=99
99 % 10 = 9
So 23673-00-9 is a valid CAS Registry Number.

23673-00-9Downstream Products

23673-00-9Relevant academic research and scientific papers

Synthesis and antihypertensive activity of some new quinazoline derivatives

Honkanen,Pippuri,Kairisalo,Nore,Karppanen,Paakkari

, p. 1433 - 1438 (2007/10/02)

A series of substituted 2-piperidino-4-amino-6,7-dimethoxyquinazolines was synthesized and screened as potential antihypertensive agents. The hypotensive effect of all the new compounds was studied after intravenous administrations in urethane-anesthetized normotensive rats. The furoylpiperazine moiety in the prazosin molecule could be replaced by a more stable substituted piperidine group without loss of the blood pressure lowering activity. However, the nature of the substituent profoundly influenced the hypotensive potency as well as the duration of the hypotensive action. Some of the new compounds were found to be as potent as prazosin. On the basis of potency and the duration of the hypotensive action in the anesthetized rats, five of the most promising compounds were selected for further studies. Each of these agents exerted an antihypertensive effect upon oral administrations in conscious spontaneously hypertensive rats. At small doses, the new compounds appeared to be somewhat less potent than prazosin, but at the higher doses of 10-100 μmol/kg, two of them appeared to be even more efficacious antihypertensive agents than prazosin.

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