1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine丨CAS 5807-14-7

1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine丨CAS 5807-14-7
Product Introduction:
Catalog No.: SS009572
CAS No.: 5807-14-7
Purity: 99% min; Assay: 97~102%
Product Name: 1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine
Molecular Formula: C7H13N3
Molecular Weight: 139.20
Synonym(s): TBD
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Technical Parameters
Description

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Specifications of 1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine丨CAS 5807-14-7

 

Appearance

White to light yellow solid

Purity

99% min

Assay

97~102%

Identification (HPLC)

The RT of main peak in sample solution should be identical with the RT of reference as related substance

Related Substances

 

1-(3-aminopropyl)-TH-pyrimidin-2(1H)-one

0.5% max

Other single impurity

0.5% max

Water

1.0% max

 

Transport Information of 1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine丨CAS 5807-14-7

 

Parameter

Specification

UN Number

1759

Class

8

Packing Group

II

H.S. Code

2932999099

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Tightly closed. Store in a closed, dry, ventilated place

Condition to Avoid

 

Package

 

 

Manufacturing Information of 1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine丨CAS 5807-14-7

 

Parameter

Specification

Capacity

1.5MT/year

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

Production since 2001

Stock

 

 

 

 

Overview

1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine丨CAS 5807-14-7 is part of the fused diazine heterocycles, specifically pyrimido[1,2-a]pyrimidines, with saturated nitrogen-rich rings that exhibit chemical versatility and biological relevance.


 

Applications

1. Pharmaceutical Intermediates

Building Block in Drug Synthesis:
Its nitrogen-rich fused ring structure makes it a useful intermediate in the synthesis of a variety of bioactive compounds, including:

Antiviral agents

Antibacterial or antifungal molecules

CNS-active compounds

Lead Structure in Medicinal Chemistry:
The compound serves as a scaffold for structure–activity relationship (SAR) studies, aiding the design of new drug candidates.

2. Agrochemical Development

Used in the synthesis of agrochemicals, such as growth regulators or pesticidal agents, especially where nitrogen heterocycles enhance activity and specificity.

3. Coordination Chemistry and Catalysis

Chelating Ligand Potential:
The nitrogen atoms in the fused ring system can act as ligands for transition metals, enabling its use in the development of metal complexes for catalysis or materials science.

4. Chemical Research

Frequently utilized in academic and industrial research as a model compound for:

Studying heterocyclic reactivity

Exploring nucleophilicity or basicity in nitrogen-containing systems

Developing novel synthesis routes for polycyclic N-heterocycles


 

Benefits

1. Structural Versatility

The fused bicyclic structure provides rigidity and electron density, making it an excellent framework for further functionalization in drug design.

2. Nitrogen-Rich Scaffold

Multiple nitrogen atoms enhance hydrogen bonding potential, metal coordination, and biological interactions.

3. Good Solubility and Stability

Water-soluble and relatively stable, which is advantageous for handling, formulation, and further reactions in aqueous or polar systems.

4. High Synthetic Utility

Its ready availability and compatibility with a range of reactions (alkylation, acylation, N-substitution) make it a flexible synthetic intermediate.


 

Conclusion

1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine丨CAS 5807-14-7 is a valuable nitrogen-containing heterocycle widely applied in pharmaceutical, agrochemical, and chemical research. Its compact, electron-rich bicyclic structure makes it ideal for building bioactive molecules and coordinating metal complexes. With broad synthetic flexibility and biological potential, it continues to be a favored tool in modern organic and medicinal chemistry.

 

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