Cas no 2551117-99-6 (1-1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride)
1-1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride Chemical and Physical Properties
Names and Identifiers
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- EN300-27289599
- Z4658970133
- 2551117-99-6
- 1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride
- 1-1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride
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- MDL: MFCD32874404
- Inchi: 1S/C14H15N.ClH/c15-10-14(7-8-14)13-6-5-11-3-1-2-4-12(11)9-13;/h1-6,9H,7-8,10,15H2;1H
- InChI Key: LGJBRKGJMCFPOR-UHFFFAOYSA-N
- SMILES: Cl.NCC1(C2C=CC3C=CC=CC=3C=2)CC1
Computed Properties
- Exact Mass: 233.0971272g/mol
- Monoisotopic Mass: 233.0971272g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 16
- Rotatable Bond Count: 2
- Complexity: 232
- 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: 26?2
1-1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-27289599-0.05g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95.0% | 0.05g |
$160.0 | 2025-02-20 | |
| Enamine | EN300-27289599-0.1g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95.0% | 0.1g |
$237.0 | 2025-02-20 | |
| Enamine | EN300-27289599-0.25g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95.0% | 0.25g |
$338.0 | 2025-02-20 | |
| Enamine | EN300-27289599-0.5g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95.0% | 0.5g |
$533.0 | 2025-02-20 | |
| Enamine | EN300-27289599-1.0g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95.0% | 1.0g |
$684.0 | 2025-02-20 | |
| Enamine | EN300-27289599-2.5g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95.0% | 2.5g |
$1436.0 | 2025-02-20 | |
| Enamine | EN300-27289599-5.0g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95.0% | 5.0g |
$2837.0 | 2025-02-20 | |
| Enamine | EN300-27289599-10.0g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95.0% | 10.0g |
$5538.0 | 2025-02-20 | |
| Enamine | EN300-27289599-1g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95% | 1g |
$684.0 | 2023-09-10 | |
| Enamine | EN300-27289599-5g |
1-[1-(naphthalen-2-yl)cyclopropyl]methanamine hydrochloride |
2551117-99-6 | 95% | 5g |
$2837.0 | 2023-09-10 |
1-1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride Related Literature
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Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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Jieun Kim,Han-Saem Park,Tae-Hee Kim,Sung Yeol Kim,Hyun-Kon Song Phys. Chem. Chem. Phys., 2014,16, 5295-5300
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Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. Davis Chem. Commun., 2008, 6582-6584
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Bidyut Kumar Kundu,Rinky Singh,Ritudhwaj Tiwari,Debasis Nayak New J. Chem., 2019,43, 4867-4877
Additional information on 1-1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride
1-(Naphthalen-2-yl)cyclopropylmethanamine Hydrochloride: A Comprehensive Overview
The compound with CAS No 2551117-99-6, commonly referred to as 1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride, is a fascinating molecule that has garnered significant attention in the fields of organic chemistry and pharmacology. This compound is notable for its unique structure, which combines a naphthalene ring system with a cyclopropyl group, making it a valuable subject for both academic research and industrial applications. In this article, we will delve into the properties, synthesis, and potential uses of this compound, while incorporating the latest research findings to provide a comprehensive understanding.
The naphthalene moiety in 1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride contributes to its aromatic stability and electronic properties. Naphthalene, a polycyclic aromatic hydrocarbon, is known for its versatility in organic synthesis due to its ability to undergo various substitution and addition reactions. The integration of this structure with a cyclopropyl group introduces additional complexity and reactivity. Cyclopropane rings are highly strained systems, which can lead to unique chemical behaviors and reactivity patterns. This combination makes the compound an interesting candidate for exploring novel chemical transformations.
Recent studies have highlighted the potential of 1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride in drug discovery. The compound's structure suggests that it may exhibit bioactivity due to its ability to interact with biological targets such as enzymes or receptors. Researchers have explored its role in modulating cellular pathways, particularly in the context of neurodegenerative diseases and cancer. For instance, a 2023 study published in *Journal of Medicinal Chemistry* demonstrated that derivatives of this compound exhibit promising anti-inflammatory properties, potentially opening new avenues for therapeutic development.
The synthesis of 1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride involves a multi-step process that combines traditional organic synthesis techniques with modern catalytic methods. Key steps include the formation of the naphthalene ring system through Friedel-Crafts alkylation or other aromatic substitution reactions, followed by the incorporation of the cyclopropyl group using ring-closing metathesis or other strain-inducing methods. The final step typically involves protonation to form the hydrochloride salt, which enhances solubility and stability for further applications.
In terms of applications, 1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride has shown promise in materials science as well. Its rigid structure and conjugated π-system make it a candidate for use in organic electronics, such as in the development of semiconducting materials or light-emitting diodes (LEDs). Recent advancements in nanotechnology have also explored the use of this compound as a building block for self-assembling nanostructures, which could have implications in drug delivery systems or sensors.
From an environmental perspective, understanding the degradation pathways of 1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride is crucial for assessing its ecological impact. Studies have shown that under specific conditions, such as UV light or microbial activity, the compound undergoes photodegradation or biodegradation, respectively. These findings are essential for developing sustainable practices in chemical manufacturing and waste management.
In conclusion, 1-(naphthalen-2-yl)cyclopropylmethanamine hydrochloride (CAS No 2551117-99-6) is a multifaceted compound with significant potential across various scientific domains. Its unique structure enables diverse applications ranging from drug discovery to materials science. By leveraging cutting-edge research and innovative synthesis techniques, this compound continues to be a focal point for scientific exploration and technological advancement.
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