Cas no 1353964-90-5 (N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride)

N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride is a synthetic organic compound featuring a thiazole ring core substituted with a chloromethyl group and a cyclopropylamine moiety, in its hydrochloride salt form. This structure confers stability and enhanced solubility, making it suitable for pharmaceutical and agrochemical applications. The chlorothiazole component provides reactivity for further derivatization, while the cyclopropylamine group contributes to steric and electronic modulation in target interactions. The hydrochloride salt improves handling and storage properties. This compound is primarily utilized as an intermediate in the synthesis of biologically active molecules, particularly in the development of antimicrobial and pesticidal agents, due to its versatile functional groups and robust chemical framework.
N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride structure
1353964-90-5 structure
Product Name:N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride
CAS No:1353964-90-5
MF:C7H10Cl2N2S
MW:225.138698101044
CID:2157614
Update Time:2025-05-27

N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • N-((2-chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride
    • AM93415
    • N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride
    • Inchi: 1S/C7H9ClN2S.ClH/c8-7-10-4-6(11-7)3-9-5-1-2-5;/h4-5,9H,1-3H2;1H
    • InChI Key: MVWSGCWTHWEFOB-UHFFFAOYSA-N
    • SMILES: ClC1=NC=C(CNC2CC2)S1.Cl

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3
  • Complexity: 140
  • Topological Polar Surface Area: 53.2

N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride Security Information

N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Fluorochem
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£458.00 2022-03-01
Chemenu
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Additional information on N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride

Comprehensive Overview of N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride (CAS 1353964-90-5)

N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride (CAS 1353964-90-5) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its unique thiazole and cyclopropylamine moieties, serves as a key intermediate in the synthesis of bioactive molecules. Its structural features make it a valuable candidate for drug discovery, particularly in targeting enzymes and receptors involved in metabolic pathways.

The growing interest in heterocyclic compounds like N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride stems from their versatility in medicinal chemistry. Researchers are increasingly exploring its potential applications in developing antimicrobial agents and anti-inflammatory drugs, aligning with current trends in combating antibiotic resistance and chronic diseases. The compound’s chlorothiazole group enhances its binding affinity to biological targets, a property highly sought after in rational drug design.

From a synthetic perspective, CAS 1353964-90-5 exemplifies the importance of scaffold diversification in modern organic chemistry. Its cyclopropanamine segment introduces steric constraints that can modulate molecular conformation, influencing pharmacokinetic profiles. This aligns with frequent search queries such as "role of cyclopropylamine in drug design" and "thiazole derivatives in medicinal chemistry", reflecting the compound’s relevance to cutting-edge research.

In agrochemical applications, derivatives of N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride have shown promise as plant growth regulators and pest control agents. The chlorothiazolyl moiety’s electron-withdrawing properties contribute to its bioactivity, addressing industry demands for sustainable crop protection solutions—a topic frequently searched in connection with "green chemistry in agriculture".

Analytical studies of CAS 1353964-90-5 emphasize its stability under physiological conditions, with HPLC and LC-MS data confirming high purity standards. These characteristics answer common technical queries like "analytical methods for amine hydrochloride salts" while supporting its utility in high-throughput screening platforms. The compound’s solubility profile further enhances its applicability in formulation development.

Recent patent literature highlights innovative uses of N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride in kinase inhibitor design, particularly for oncology targets. This connects with trending searches on "next-generation cancer therapeutics", demonstrating how this molecular scaffold bridges academic research and industrial innovation. Computational modeling studies predict favorable ADMET properties for its derivatives.

Environmental considerations regarding chlorinated heterocycles have led to improved synthetic protocols for CAS 1353964-90-5, reducing hazardous byproducts. Such advancements respond to growing concerns about "green synthesis of pharmaceutical intermediates", making this compound a case study in sustainable chemical production.

The crystalline nature of N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride facilitates precise X-ray diffraction analysis, providing structural insights valuable for structure-activity relationship (SAR) studies. Researchers frequently investigate "crystallography of amine salts" to optimize molecular interactions, further underscoring this compound’s scientific significance.

As regulatory agencies emphasize quality by design (QbD) principles, the well-characterized properties of CAS 1353964-90-5 make it an exemplary subject for process chemistry optimization. This addresses industry searches for "scale-up strategies for complex amines" while ensuring reproducible synthetic outcomes.

In conclusion, N-((2-Chlorothiazol-5-yl)methyl)cyclopropanamine hydrochloride represents a multifaceted tool for researchers exploring bioactive small molecules. Its structural complexity and demonstrated applications across therapeutic and agricultural domains position it as a compound of enduring scientific and commercial interest.

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