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1H-PYRROLO[2,3-D]PYRIMIDIN-2(7H)-ONE, with the molecular formula C7H5N3O, is a heterocyclic compound characterized by a pyrrole ring fused to a pyrimidine ring, featuring an oxygen atom at the 2-position of the pyrrolo ring. This unique structure endows it with potential biological activity, making it a subject of interest for pharmaceutical research and development, particularly as an anticancer agent. Additionally, it serves as a building block in organic synthesis for creating more complex molecules.

322728-22-3

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322728-22-3 Usage

Uses

Used in Pharmaceutical Industry:
1H-PYRROLO[2,3-D]PYRIMIDIN-2(7H)-ONE is used as a pharmaceutical agent for its potential anticancer properties. Its unique structure allows it to be studied for interactions with biological targets, offering a promising avenue for the development of new cancer therapies.
Used in Organic Synthesis:
In the field of organic synthesis, 1H-PYRROLO[2,3-D]PYRIMIDIN-2(7H)-ONE is utilized as a key building block. Its incorporation into more complex molecular structures facilitates the creation of a variety of compounds with diverse applications, including but not limited to pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 322728-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,2,7,2 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 322728-22:
(8*3)+(7*2)+(6*2)+(5*7)+(4*2)+(3*8)+(2*2)+(1*2)=123
123 % 10 = 3
So 322728-22-3 is a valid CAS Registry Number.

322728-22-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-PYRROLO[2,3-D]PYRIMIDIN-2(7H)-ONE

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:322728-22-3 SDS

322728-22-3Relevant academic research and scientific papers

1,N6-Etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides

Seela, Frank,Schweinberger, Enno,Xu, Kuiying,Sirivolu, Venkata Ramana,Rosemeyer, Helmut,Becker, Eva-Maria

, p. 3471 - 3482 (2007/10/03)

The synthesis of 1,N6-etheno-7-deaza-2′-deoxyadenosine (12b) which was prepared from 7-deaza-2′-deoxyadenosine (5a) with chloroacetaldehyde is described. Also the regioselective glycosylation of the 7-deazapurine-2-one at nitrogen-1 (19) furnis

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