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322728-22-3

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322728-22-3 Usage

General Description

1H-Pyrrolo[2,3-d]pyrimidin-2(7H)-one is a chemical compound with the molecular formula C7H5N3O. It is a heterocyclic compound that consists of a pyrrole ring fused to a pyrimidine ring, with an oxygen atom attached at the 2-position of the pyrrolo ring. 1H-PYRROLO[2,3-D]PYRIMIDIN-2(7H)-ONE has potential biological activity and is being studied for its potential pharmaceutical applications, including as an anticancer agent. It is also used in organic synthesis as a building block for more complex molecules. 1H-Pyrrolo[2,3-d]pyrimidin-2(7H)-one has a unique structure and properties that make it of interest for further research and development in various fields.

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:322728-22-3 SDS

322728-22-3Relevant articles and documents

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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