Cas no 1093403-67-8 (N-(1,2-dimethylpropyl)cyclopropanamine;hydrochloride)

N-(1,2-Dimethylpropyl)cyclopropanamine hydrochloride is a cyclopropylamine derivative with potential applications in pharmaceutical and organic synthesis. The compound features a cyclopropylamine moiety bound to a branched alkyl chain, enhancing its steric and electronic properties. The hydrochloride salt form improves stability and solubility, facilitating handling and storage. This structural configuration may be of interest in medicinal chemistry for the development of bioactive molecules, particularly due to the cyclopropane ring's conformational rigidity and the amine group's reactivity. Its well-defined molecular structure allows for precise modifications, making it a valuable intermediate in targeted synthetic pathways. Suitable for research and development under controlled conditions.
N-(1,2-dimethylpropyl)cyclopropanamine;hydrochloride structure
1093403-67-8 structure
Product Name:N-(1,2-dimethylpropyl)cyclopropanamine;hydrochloride
CAS No:1093403-67-8
MF:C8H18ClN
MW:163.68822145462
MDL:MFCD09971421
CID:4571064
Update Time:2025-10-29

N-(1,2-dimethylpropyl)cyclopropanamine;hydrochloride Chemical and Physical Properties

Names and Identifiers

    • N-(3-methylbutan-2-yl)cyclopropanamine hydrochloride
    • N-(1,2-dimethylpropyl)cyclopropanamine;hydrochloride
    • MDL: MFCD09971421
    • Inchi: 1S/C8H17N.ClH/c1-6(2)7(3)9-8-4-5-8;/h6-9H,4-5H2,1-3H3;1H
    • InChI Key: RWNDCEXRJHOGBX-UHFFFAOYSA-N
    • SMILES: N(C1CC1)C(C)C(C)C.Cl

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Additional information on N-(1,2-dimethylpropyl)cyclopropanamine;hydrochloride

Introduction to N-(1,2-dimethylpropyl)cyclopropanamine Hydrochloride (CAS No. 1093403-67-8)

N-(1,2-dimethylpropyl)cyclopropanamine hydrochloride is a chemical compound that has garnered significant attention in the field of pharmaceutical research and development. This compound, with the CAS number 1093403-67-8, belongs to a class of molecules that exhibit intriguing pharmacological properties. The hydrochloride salt form of this compound enhances its solubility in aqueous solutions, making it more suitable for various biomedical applications.

The molecular structure of N-(1,2-dimethylpropyl)cyclopropanamine hydrochloride consists of a cyclopropane ring substituted with a 1,2-dimethylpropyl group and an amine functional group, which is further converted into its hydrochloride salt. This unique structural arrangement contributes to its distinct chemical and biological characteristics. The cyclopropane ring is known for its high reactivity and stability, while the amine group provides a site for further chemical modifications and interactions with biological targets.

In recent years, there has been growing interest in exploring the potential of cyclopropane derivatives as pharmacological agents. The compound N-(1,2-dimethylpropyl)cyclopropanamine hydrochloride has been studied for its potential role in modulating various biological pathways. Research indicates that this compound may interact with specific enzymes and receptors, leading to therapeutic effects. For instance, studies have suggested that it might have anti-inflammatory properties by inhibiting the activity of certain inflammatory mediators.

One of the most compelling aspects of N-(1,2-dimethylpropyl)cyclopropanamine hydrochloride is its ability to cross the blood-brain barrier, which is crucial for many central nervous system (CNS) drugs. This property makes it an attractive candidate for developing treatments for neurological disorders. Current research is focusing on understanding how this compound interacts with CNS receptors and whether it can be used to alleviate symptoms associated with conditions such as depression and anxiety.

The synthesis of N-(1,2-dimethylpropyl)cyclopropanamine hydrochloride involves multi-step organic reactions that require precise control over reaction conditions. The process typically begins with the formation of the cyclopropane ring followed by the introduction of the 1,2-dimethylpropyl group and the amine functional group. The final step involves converting the free amine into its hydrochloride salt to improve solubility and stability. Advanced synthetic techniques have been employed to optimize yield and purity, ensuring that the final product meets pharmaceutical standards.

Evaluation of the pharmacokinetic properties of N-(1,2-dimethylpropyl)cyclopropanamine hydrochloride has revealed interesting findings regarding its absorption, distribution, metabolism, and excretion (ADME). Studies have shown that this compound exhibits moderate oral bioavailability and a relatively long half-life, suggesting potential for once-daily dosing in therapeutic applications. Additionally, preliminary toxicology studies indicate that it is well-tolerated at moderate doses, although further research is needed to fully assess its safety profile.

The potential therapeutic applications of N-(1,2-dimethylpropyl)cyclopropanamine hydrochloride extend beyond CNS disorders. Research is ongoing to explore its efficacy in treating conditions such as pain syndromes and autoimmune diseases. The compound's ability to modulate inflammatory pathways makes it a promising candidate for developing novel anti-inflammatory agents. Moreover, its structural features may allow it to interact with other biological targets, opening up possibilities for treating a wide range of diseases.

In conclusion, N-(1,2-dimethylpropyl)cyclopropanamine hydrochloride (CAS No. 1093403-67-8) is a fascinating compound with significant potential in pharmaceutical applications. Its unique molecular structure and pharmacological properties make it an attractive candidate for further research and development. As our understanding of its mechanisms of action continues to grow, so too does the likelihood that it will play a crucial role in future medical treatments.

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