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Pyrido[1,2-a]pyrimidin-4-one is a heterocyclic chemical compound characterized by a fused pyrimidine structure. It is a member of the alkaloid group, typically sourced from natural origins such as plants and microorganisms. Pyrido[1,2-a]pyriMidin-4-one exhibits a range of potential biological activities, making it a valuable asset in the pharmaceutical industry for the innovation of novel drugs. Its unique chemical structure and properties render it suitable for diverse medicinal applications, encompassing anti-inflammatory, anti-tumor, and anti-bacterial capabilities. Pyrido[1,2-a]pyrimidin-4-one stands as a multifaceted compound with significant potential in medical research and drug development.

23443-10-9

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23443-10-9 Usage

Uses

Used in Pharmaceutical Industry:
Pyrido[1,2-a]pyrimidin-4-one is utilized as a key component in drug development for its diverse biological activities. It serves as a foundation for creating new medications targeting various health conditions due to its anti-inflammatory, anti-tumor, and anti-bacterial properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, Pyrido[1,2-a]pyrimidin-4-one is employed as a scaffold for designing and synthesizing new compounds with improved pharmacological profiles. Its structural attributes allow for modifications that can enhance the efficacy and selectivity of drugs, contributing to the advancement of personalized medicine.
Used in Drug Discovery:
Pyrido[1,2-a]pyrimidin-4-one is leveraged in drug discovery processes to identify lead compounds with therapeutic potential. Its presence in natural sources and demonstrated biological activities make it an attractive candidate for high-throughput screening and further optimization to treat a spectrum of diseases.
Used in Natural Product Chemistry:
As a naturally occurring compound, Pyrido[1,2-a]pyrimidin-4-one is used in the study of natural product chemistry to understand its biosynthetic pathways and ecological roles. This knowledge can inform the development of sustainable methods for its production and application in medicine.
Each application underscores the versatility and significance of Pyrido[1,2-a]pyrimidin-4-one in the realm of pharmaceuticals and medicine, highlighting its multifaceted utility in addressing contemporary health challenges.

Check Digit Verification of cas no

The CAS Registry Mumber 23443-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,4 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23443-10:
(7*2)+(6*3)+(5*4)+(4*4)+(3*3)+(2*1)+(1*0)=79
79 % 10 = 9
So 23443-10-9 is a valid CAS Registry Number.

23443-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name pyrido[1,2-a]pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 4H-Pyrido[1,2-a]pyrimidin-4-one

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 -
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More Details:23443-10-9 SDS

23443-10-9Relevant academic research and scientific papers

Suzuki-Miyaura cross-coupling reactions of halo derivatives of 4H-pyrido[1,2-a]pyrimidin-4-ones

Molnar, Annamaria,Kapros, Anita,Parkanyi, Laszlo,Mucsi, Zoltan,Vlad, Gabor,Hermecz, Istvan

supporting information; experimental part, p. 6559 - 6565 (2011/11/05)

The palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of halo derivatives of 4H-pyrido[1,2-a]pyrimidin-4-one with (het)arylboronic acids allow easy access to (het)aryl and vinyl derivatives of this bicycle in good to excellent yields, even from chloro derivatives. The sequence of reactivity of the halogen in the different positions of the ring system was also investigated. 6-Phenyl-4H-pyrido[1,2-a]pyrimidin-4-one could be prepared by thermal cyclization of isopropylidene (6-phenylpyrid-2-ylamino)methylenemalonate, together with a small amount of 7-phenyl-1,4-dihydro-1,8-naphthyridin-4-one.

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