Cas no 2060000-69-1 ((2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride)

(2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride structure
2060000-69-1 structure
Product Name:(2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride
CAS No:2060000-69-1
MF:C12H18ClN
MW:211.731022357941
MDL:MFCD30497531
CID:4635372
PubChem ID:134690766
Update Time:2025-10-29

(2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • (2,2-dimethyl-1-phenylcyclopropyl)methanamine hydrochloride
    • E73029
    • (2,2-dimethyl-1-phenylcyclopropyl)methanamine;hydrochloride
    • (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride
    • MDL: MFCD30497531
    • Inchi: 1S/C12H17N.ClH/c1-11(2)8-12(11,9-13)10-6-4-3-5-7-10;/h3-7H,8-9,13H2,1-2H3;1H
    • InChI Key: ADIOXIBZWVSWIJ-UHFFFAOYSA-N
    • SMILES: Cl.NCC1(C2C=CC=CC=2)CC1(C)C

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 191
  • Topological Polar Surface Area: 26

(2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride Pricemore >>

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Additional information on (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride

Comprehensive Overview of (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride (CAS No. 2060000-69-1)

(2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride is a specialized organic compound with the CAS number 2060000-69-1. This compound belongs to the class of cyclopropylamine derivatives, which are known for their unique structural and chemical properties. The presence of the phenyl and dimethylcyclopropyl groups in its structure makes it a subject of interest in various research and industrial applications. The hydrochloride salt form enhances its stability and solubility, making it suitable for a wide range of uses.

The molecular formula of (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride is C12H18ClN, and it has a molecular weight of approximately 203.73 g/mol. The compound's structure features a cyclopropane ring substituted with two methyl groups and a phenyl group, along with an amine functional group. This configuration contributes to its unique reactivity and potential applications in medicinal chemistry, material science, and other fields.

One of the key reasons for the growing interest in (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride is its potential role in the development of novel pharmaceuticals. Cyclopropylamine derivatives are often explored for their bioactivity, and this compound is no exception. Researchers are investigating its potential as a building block for drugs targeting neurological disorders, given the amine group's ability to interact with biological systems. The phenyl group further enhances its lipophilicity, which can improve membrane permeability—a critical factor in drug design.

In addition to pharmaceutical applications, (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride is also being studied for its use in material science. The cyclopropyl ring is known for its strain energy, which can impart unique mechanical properties to polymers and other materials. This makes the compound a candidate for developing high-performance materials with tailored characteristics. Its stability under various conditions further adds to its appeal in industrial applications.

The synthesis of (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride typically involves multi-step organic reactions, starting from readily available precursors. One common approach is the reaction of 1-phenylcyclopropane with formaldehyde and dimethylamine, followed by hydrochlorination to yield the final product. The process requires careful control of reaction conditions to ensure high purity and yield. Advanced analytical techniques such as NMR, HPLC, and mass spectrometry are employed to characterize the compound and confirm its identity.

From a market perspective, the demand for (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride is driven by its versatility and potential applications. Pharmaceutical companies and research institutions are the primary consumers, using it as an intermediate in drug discovery programs. The compound's unique structure also makes it a valuable tool for academic research, particularly in studies focusing on small molecule interactions and structure-activity relationships.

Safety and handling of (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride are critical considerations. While it is not classified as a hazardous material, standard laboratory precautions should be followed. Proper storage conditions, including protection from moisture and light, are essential to maintain its stability. Researchers and industrial users should also adhere to local regulations regarding chemical handling and disposal.

In recent years, the compound has garnered attention in the context of green chemistry and sustainable synthesis. Efforts are underway to develop more environmentally friendly routes for its production, minimizing waste and energy consumption. This aligns with the broader trend in the chemical industry toward sustainable practices and reduced environmental impact.

Looking ahead, the future of (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride appears promising. Ongoing research into its pharmacological properties and material applications could unlock new opportunities. As the scientific community continues to explore the potential of cyclopropylamine derivatives, this compound is likely to remain a focal point of innovation and discovery.

For those interested in sourcing (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride, it is available through specialized chemical suppliers. Buyers should ensure they procure the compound from reputable sources to guarantee quality and purity. Certificates of analysis and detailed technical data sheets are typically provided to support its use in research and industrial applications.

In summary, (2,2-Dimethyl-1-phenylcyclopropyl)methanamine hydrochloride (CAS No. 2060000-69-1) is a versatile and valuable compound with significant potential in pharmaceuticals, material science, and beyond. Its unique structural features and reactivity make it a subject of ongoing research and development, promising exciting advancements in the years to come.

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