Cas no 2007908-73-6 (2,4-Dichloropyrimidin-5-amine hydrochloride)

2,4-Dichloropyrimidin-5-amine hydrochloride is a versatile heterocyclic compound widely used as a key intermediate in pharmaceutical and agrochemical synthesis. Its reactive dichloropyrimidine core allows for selective functionalization, enabling the construction of complex molecular architectures. The hydrochloride salt form enhances stability and solubility, facilitating handling and storage. This compound is particularly valuable in medicinal chemistry for the development of kinase inhibitors and other biologically active molecules due to its ability to undergo nucleophilic substitution reactions at the 2- and 4-positions. Its consistent purity and well-characterized properties make it a reliable building block for research and industrial applications.
2,4-Dichloropyrimidin-5-amine hydrochloride structure
2007908-73-6 structure
Product Name:2,4-Dichloropyrimidin-5-amine hydrochloride
CAS No:2007908-73-6
MF:C4H4Cl3N3
MW:200.453657150269
CID:4671341
PubChem ID:92132814
Update Time:2025-11-02

2,4-Dichloropyrimidin-5-amine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2,4-Dichloropyrimidin-5-amine hydrochloride
    • AX8278196
    • O10597
    • 2,4-Dichloropyrimidin-5-aminehydrochloride
    • CS-0435640
    • 2007908-73-6
    • 2,4-DICHLOROPYRIMIDIN-5-AMINE HCL
    • Inchi: 1S/C4H3Cl2N3.ClH/c5-3-2(7)1-8-4(6)9-3;/h1H,7H2;1H
    • InChI Key: WRSBYRJSROHFSX-UHFFFAOYSA-N
    • SMILES: ClC1C(=CN=C(N=1)Cl)N.Cl

Computed Properties

  • Exact Mass: 198.947080g/mol
  • Monoisotopic Mass: 198.947080g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 99.8
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 51.8

2,4-Dichloropyrimidin-5-amine hydrochloride Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd.
D95790-1g
2,4-Dichloropyrimidin-5-amine hydrochloride
2007908-73-6 95%
1g
¥622.0 2023-09-08
SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd.
D95790-5g
2,4-Dichloropyrimidin-5-amine hydrochloride
2007908-73-6 95%
5g
¥1822.0 2023-09-08

Additional information on 2,4-Dichloropyrimidin-5-amine hydrochloride

Comprehensive Overview of 2,4-Dichloropyrimidin-5-amine hydrochloride (CAS No. 2007908-73-6)

2,4-Dichloropyrimidin-5-amine hydrochloride (CAS No. 2007908-73-6) is a specialized chemical compound widely utilized in pharmaceutical research and organic synthesis. This compound belongs to the pyrimidine family, which is known for its significance in drug development and agrochemical applications. The presence of chlorine atoms at the 2 and 4 positions, along with an amine group at the 5 position, makes it a versatile intermediate for further chemical modifications. Researchers and industries value this compound for its potential in creating novel therapeutic agents and its role in advanced synthetic pathways.

The chemical structure of 2,4-Dichloropyrimidin-5-amine hydrochloride features a pyrimidine ring, a heterocyclic aromatic compound that is a cornerstone in medicinal chemistry. The hydrochloride salt form enhances its stability and solubility, making it easier to handle in laboratory settings. This compound is particularly relevant in the context of current trends in drug discovery and precision medicine, where heterocyclic compounds play a pivotal role. Its applications extend to the development of kinase inhibitors, antiviral agents, and other bioactive molecules, aligning with the growing demand for targeted therapies.

One of the key reasons for the popularity of 2,4-Dichloropyrimidin-5-amine hydrochloride in research is its reactivity. The chlorine atoms are excellent leaving groups, facilitating nucleophilic substitution reactions, which are fundamental in constructing complex molecular architectures. This property is especially valuable in the synthesis of small-molecule drugs, a rapidly expanding area in the pharmaceutical industry. Additionally, the amine group provides a site for further functionalization, enabling the creation of diverse derivatives with potential biological activity.

In recent years, the demand for pyrimidine derivatives like 2,4-Dichloropyrimidin-5-amine hydrochloride has surged due to their role in addressing global health challenges. For instance, pyrimidine-based compounds have been investigated for their efficacy against emerging viral infections, a topic of significant interest in the wake of recent pandemics. Researchers are also exploring their use in cancer treatment, where kinase inhibitors derived from pyrimidine scaffolds have shown promise in clinical trials. These applications highlight the compound's relevance in contemporary biomedical research.

The synthesis and handling of 2,4-Dichloropyrimidin-5-amine hydrochloride require adherence to standard laboratory protocols to ensure safety and reproducibility. While the compound itself is not classified as hazardous under normal conditions, proper precautions, such as the use of personal protective equipment (PPE) and adequate ventilation, are recommended. Its storage should be in a cool, dry place, away from incompatible substances, to maintain its integrity over time. These guidelines are essential for researchers and manufacturers working with this compound.

From a commercial perspective, 2,4-Dichloropyrimidin-5-amine hydrochloride is available through specialized chemical suppliers catering to the pharmaceutical and biotechnology sectors. The compound's market dynamics are influenced by the increasing investment in drug discovery and the expansion of contract research organizations (CROs). As the demand for high-quality intermediates grows, suppliers are focusing on ensuring consistent purity and scalability to meet the needs of their clients. This trend underscores the compound's importance in the broader chemical supply chain.

In summary, 2,4-Dichloropyrimidin-5-amine hydrochloride (CAS No. 2007908-73-6) is a critical building block in modern chemistry, with wide-ranging applications in drug development and organic synthesis. Its unique structural features and reactivity make it a valuable tool for researchers aiming to innovate in the fields of medicine and biotechnology. As scientific advancements continue to drive the exploration of new therapeutic agents, compounds like this will remain at the forefront of chemical research, contributing to breakthroughs that address pressing global health challenges.

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