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2-nitrooxypropyl 2-(3-nitrobenzylidene) acetoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

152809-64-8

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152809-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152809-64-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,8,0 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 152809-64:
(8*1)+(7*5)+(6*2)+(5*8)+(4*0)+(3*9)+(2*6)+(1*4)=138
138 % 10 = 8
So 152809-64-8 is a valid CAS Registry Number.

152809-64-8Downstream Products

152809-64-8Relevant academic research and scientific papers

Synthesis and antihypertensive activities of new 1,4-dihydropyridine derivatives containing nitrooxyalkylester moieties at the 3- and 5-positions

Ogawa,Nakazato,Tsuchida,Hatayama

, p. 1049 - 1054 (1993)

We have synthesized new 1,4-dihydropyridine derivatives having nitrooxyalkylester moieties at the 3- and 5-positions in order to develop potent and long-lasting vasodilators. The antihypertensive activities of these compounds were compared with that of nifedipine. One of them, 2- nitrooxypropyl 3-nitrooxypropyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydro- 3,5-pyridinedicarboxylate (CD-349) was selected for further development. The structure-activity relationship is discussed.

Novel 2-amino-1,4-dihydropyridine calcium antagonists. I. Synthesis and antihypertensive effects of 2-amino-1,4-dihydropyridine derivatives having nitroxyalkoxycarbonyl groups at 3- and/or 5-position

Kobayashi,Inoue,Kita,Yoshiya,Nishino,Oizumi,Kimura

, p. 788 - 796 (2007/10/02)

Novel 2-amino-1,4-dihydropyridine derivatives, which contain nitroxy-alkoxycarbonyl groups at the 3- and/or 5-position, were synthesized and their pharmaceutical effect was evaluated in spontaneously hypertensive rats. The structure-activity relationships are discussed in terms of potency, onset-rapidity, and duration of antihypertensive activity. Remarkably prolonged duration of antihypertensive action was observed when a tertiary amino group was introduced on either side of an ester chain.

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