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(2-Pyridin-2-yl-pyrimidin-4-yl)-hydrazine, also known as PDPH, is a hydrazine derivative with a molecular formula of C10H10N6. It features a pyridine and pyrimidine ring structure, classifying it as a heterocyclic compound. PDPH has demonstrated potential anticancer activity by inhibiting kinase enzymes that play a role in cell proliferation. Furthermore, it has been considered for therapeutic applications in treating neurodegenerative disorders and as a building block for synthesizing other biologically active compounds. This makes PDPH a versatile chemical with promising applications in medicine and pharmaceuticals.

97603-53-7

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97603-53-7 Usage

Uses

Used in Pharmaceutical Industry:
PDPH is used as a potential anticancer agent for its ability to inhibit kinase enzymes involved in cell proliferation, offering a therapeutic approach to combat cancer.
Used in Neurodegenerative Disorder Treatment:
PDPH is utilized as a potential therapeutic agent for treating various neurodegenerative disorders, highlighting its potential in addressing neurological conditions.
Used in Synthesis of Biologically Active Compounds:
PDPH serves as a building block for the synthesis of other biologically active compounds, contributing to the development of new pharmaceuticals and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 97603-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,0 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97603-53:
(7*9)+(6*7)+(5*6)+(4*0)+(3*3)+(2*5)+(1*3)=157
157 % 10 = 7
So 97603-53-7 is a valid CAS Registry Number.

97603-53-7Downstream Products

97603-53-7Relevant academic research and scientific papers

Preparation of Triazolopyrimidines as Potential Antiasthma Agents

Medwid, Jeffrey B.,Paul, Rolf,Baker, Jannie S.,Brockman, John A.,Du, Mila T.,et al.

, p. 1230 - 1241 (2007/10/02)

With the use of the human basophil histamine release assay, 5-aryl-2-aminotriazolopyrimidines were found to be active as mediator release inhibitors.These compounds were prepared by reacting arylamidines with sodium ethyl formylacetate or with ethyl propiolate to give pyrimidinones.Treatment with phosphorus oxychloride gave a chloropyrimidine, which was converted to a hydrazinopyrimidine with hydrazine.Cyclization, using cyanogen bromide, gave the triazolopyrimidines, after a Dimroth rearrangement.Following a structure-activity evaluation, the5--2-amino (8-10), 5-(3-bromophenyl)-2-amino (8-13), 5--2-amino (8-11), and 5-(4-pyridinyl)-2-amino (6-7) compounds were found to have the best activity.They were chosen for further pharmacological and toxicological study.

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