Cas no 7043-09-6 (4,6-Dichloro-2-cyclopropylpyrimidine)

4,6-Dichloro-2-cyclopropylpyrimidine is a versatile heterocyclic compound featuring a pyrimidine core substituted with chlorine atoms at the 4 and 6 positions and a cyclopropyl group at the 2 position. This structure imparts significant reactivity, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The dichloro substitution enhances electrophilicity, facilitating nucleophilic aromatic substitution reactions, while the cyclopropyl group contributes steric and electronic effects that can influence the selectivity of downstream transformations. Its well-defined reactivity profile and stability under standard handling conditions make it suitable for use in multi-step synthetic routes, particularly in the development of biologically active molecules.
4,6-Dichloro-2-cyclopropylpyrimidine structure
7043-09-6 structure
Product Name:4,6-Dichloro-2-cyclopropylpyrimidine
CAS No:7043-09-6
MF:C7H6Cl2N2
MW:189.041939258575
MDL:MFCD11046809
CID:1026718
PubChem ID:24903687
Update Time:2025-06-25

4,6-Dichloro-2-cyclopropylpyrimidine Chemical and Physical Properties

Names and Identifiers

    • 4,6-Dichloro-2-cyclopropylpyrimidine
    • C7H6Cl2N2
    • 2-cyclopropyl-4,6-dichloropyrimidine
    • 2-Cyclopropyl-4,6-dichlorpyrimidin
    • 4,6-dichloro-2-cyclopropyl-pyrimidine
    • AC1Q3IAR
    • AG-L-24152
    • ANW-55930
    • CTK5D2384
    • QC-9232
    • N-Benzyl-4-chloroacetamide
    • YBOWZANEONZCOL-UHFFFAOYSA-N
    • 2-cyclopropyl-4,6-dichloropyrimidine;
    • 4,6-dichloro-2-cyclopropylpyrimidine;
    • RL04701
    • EBD1179797
    • SB11913
    • 4,6-dichloro-2-cyclopropyl-pyrimidine;
    • Z5053
    • F
    • DTXSID70647966
    • MFCD11046809
    • AKOS012923442
    • SCHEMBL1286211
    • 4 pound not6-Dichloro-2-cyclopropylpyrimidine
    • AM9778
    • 7043-09-6
    • Z1140391403
    • FT-0654719
    • EN300-111202
    • A836883
    • SY102645
    • GS-5842
    • CS-W003931
    • DB-074304
    • MDL: MFCD11046809
    • Inchi: 1S/C7H6Cl2N2/c8-5-3-6(9)11-7(10-5)4-1-2-4/h3-4H,1-2H2
    • InChI Key: YBOWZANEONZCOL-UHFFFAOYSA-N
    • SMILES: ClC1=CC(=NC(C2CC2)=N1)Cl

Computed Properties

  • Exact Mass: 187.99098
  • Monoisotopic Mass: 187.9908036g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 139
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 25.8
  • XLogP3: 2.7

Experimental Properties

  • PSA: 25.78

4,6-Dichloro-2-cyclopropylpyrimidine Security Information

  • HazardClass:IRRITANT

4,6-Dichloro-2-cyclopropylpyrimidine Pricemore >>

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Additional information on 4,6-Dichloro-2-cyclopropylpyrimidine

Comprehensive Guide to 4,6-Dichloro-2-cyclopropylpyrimidine (CAS No. 7043-09-6): Properties, Applications, and Industry Insights

4,6-Dichloro-2-cyclopropylpyrimidine (CAS No. 7043-09-6) is a versatile heterocyclic compound widely utilized in pharmaceutical and agrochemical research. Its molecular structure, featuring a pyrimidine ring substituted with chlorine atoms and a cyclopropyl group, makes it a critical intermediate for synthesizing bioactive molecules. With the growing demand for small-molecule drugs and crop protection agents, this compound has garnered significant attention in recent years.

The compound’s chemical stability and reactivity enable its use in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig reactions, which are pivotal in modern drug discovery. Researchers frequently search for "4,6-Dichloro-2-cyclopropylpyrimidine synthesis" or "CAS 7043-09-6 applications" to explore its role in developing kinase inhibitors and antiviral agents. Notably, its derivatives have shown promise in targeting EGFR and CDK pathways, aligning with the trending focus on precision medicine.

From an industrial perspective, 7043-09-6 is often discussed in forums about green chemistry and sustainable synthesis. Questions like "How to optimize the yield of 4,6-Dichloro-2-cyclopropylpyrimidine?" reflect the need for eco-friendly production methods. Advances in catalytic processes and solvent-free reactions have been proposed to address these challenges, catering to the pharmaceutical industry’s sustainability goals.

In agrochemical applications, this compound serves as a precursor for herbicides and fungicides, addressing global concerns about food security and crop resilience. Searches for "4,6-Dichloro-2-cyclopropylpyrimidine in agriculture" highlight its potential in combating plant pathogens resistant to conventional treatments. Its mode of action involves disrupting pyrimidine metabolism in pests, a mechanism increasingly studied for low-toxicity solutions.

Analytical techniques like HPLC, NMR, and mass spectrometry are essential for characterizing CAS 7043-09-6, ensuring purity and consistency in research. Queries such as "How to analyze 4,6-Dichloro-2-cyclopropylpyrimidine?" underscore the importance of robust quality control protocols. Regulatory compliance, including REACH and GMP standards, further drives the demand for high-purity batches in commercial-scale production.

Emerging trends in AI-driven drug discovery have also spotlighted 4,6-Dichloro-2-cyclopropylpyrimidine as a scaffold for virtual screening. Computational models predict its derivatives’ binding affinities, accelerating the identification of novel therapeutics. This synergy between wet-lab chemistry and in silico tools exemplifies the compound’s relevance in cutting-edge research.

In summary, 4,6-Dichloro-2-cyclopropylpyrimidine (CAS No. 7043-09-6) bridges multiple disciplines, from medicinal chemistry to sustainable agriculture. Its adaptability to modern synthetic challenges and alignment with industry trends ensure its continued prominence in scientific and industrial applications.

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