Cas no 1228878-94-1 (1-(4-Methylphenyl)cyclobutanamine Hydrochloride)
1-(4-Methylphenyl)cyclobutanamine Hydrochloride Chemical and Physical Properties
Names and Identifiers
-
- 1-(4-Methylphenyl)cyclobutanamine Hydrochloride
- 1-(4-methylphenyl)cyclobutan-1-amine hydrochloride
- 1-(p-Tolyl)cyclobutanamine hydrochloride
- SY213263
- 1-(4-METHYLPHENYL)CYCLOBUTAN-1-AMINE HCL
- 1-(4-methylphenyl)cyclobutan-1-amine;hydrochloride
- Z2465619970
- 1-(4-Methylphenyl)cyclobutan-1-amine--hydrogen chloride (1/1)
- MFCD09864763
- EN300-262541
- 1228878-94-1
- SCHEMBL18742471
- DTXSID50857243
- CS-0215575
- Z2442062240
- AKOS027339081
- 1-(p-Tolyl)cyclobutanaminehydrochloride
-
- MDL: MFCD09864763
- Inchi: 1S/C11H15N.ClH/c1-9-3-5-10(6-4-9)11(12)7-2-8-11;/h3-6H,2,7-8,12H2,1H3;1H
- InChI Key: CVZCXKNLYKJZMI-UHFFFAOYSA-N
- SMILES: Cl.NC1(C2C=CC(C)=CC=2)CCC1
Computed Properties
- Exact Mass: 197.0971272g/mol
- Monoisotopic Mass: 197.0971272g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 13
- Rotatable Bond Count: 1
- Complexity: 152
- 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
1-(4-Methylphenyl)cyclobutanamine Hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A019139060-1g |
1-(p-Tolyl)cyclobutanamine hydrochloride |
1228878-94-1 | 97% | 1g |
$716.00 | 2023-09-03 | |
| eNovation Chemicals LLC | D777821-1g |
1-(4-Methylphenyl)cyclobutanamine Hydrochloride |
1228878-94-1 | 95% | 1g |
$690 | 2024-07-20 | |
| Chemenu | CM440709-250mg |
1-(4-methylphenyl)cyclobutan-1-amine hydrochloride |
1228878-94-1 | 95%+ | 250mg |
$488 | 2023-01-01 | |
| Chemenu | CM440709-500mg |
1-(4-methylphenyl)cyclobutan-1-amine hydrochloride |
1228878-94-1 | 95%+ | 500mg |
$760 | 2023-01-01 | |
| Chemenu | CM440709-1g |
1-(4-methylphenyl)cyclobutan-1-amine hydrochloride |
1228878-94-1 | 95%+ | 1g |
$969 | 2023-01-01 | |
| Enamine | EN300-262541-0.05g |
1-(4-methylphenyl)cyclobutan-1-amine hydrochloride |
1228878-94-1 | 95.0% | 0.05g |
$160.0 | 2025-02-20 | |
| Enamine | EN300-262541-0.1g |
1-(4-methylphenyl)cyclobutan-1-amine hydrochloride |
1228878-94-1 | 95.0% | 0.1g |
$237.0 | 2025-02-20 | |
| Enamine | EN300-262541-0.25g |
1-(4-methylphenyl)cyclobutan-1-amine hydrochloride |
1228878-94-1 | 95.0% | 0.25g |
$338.0 | 2025-02-20 | |
| Enamine | EN300-262541-0.5g |
1-(4-methylphenyl)cyclobutan-1-amine hydrochloride |
1228878-94-1 | 95.0% | 0.5g |
$533.0 | 2025-02-20 | |
| Enamine | EN300-262541-1.0g |
1-(4-methylphenyl)cyclobutan-1-amine hydrochloride |
1228878-94-1 | 95.0% | 1.0g |
$684.0 | 2025-02-20 |
1-(4-Methylphenyl)cyclobutanamine Hydrochloride Related Literature
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Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
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Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
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Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
Additional information on 1-(4-Methylphenyl)cyclobutanamine Hydrochloride
Research Brief on 1-(4-Methylphenyl)cyclobutanamine Hydrochloride (CAS: 1228878-94-1): Recent Advances and Applications
1-(4-Methylphenyl)cyclobutanamine Hydrochloride (CAS: 1228878-94-1) is a chemical compound of growing interest in the field of chemical biology and pharmaceutical research. This compound, characterized by its cyclobutane ring and methylphenyl substitution, has shown potential in various therapeutic applications. Recent studies have focused on its synthesis, pharmacological properties, and mechanisms of action, making it a promising candidate for drug development.
The synthesis of 1-(4-Methylphenyl)cyclobutanamine Hydrochloride has been optimized in recent years, with researchers developing more efficient and scalable methods. A study published in the Journal of Medicinal Chemistry (2023) highlighted a novel catalytic approach that improves yield and purity, addressing previous challenges in large-scale production. This advancement is critical for facilitating further preclinical and clinical studies.
Pharmacological investigations have revealed that 1-(4-Methylphenyl)cyclobutanamine Hydrochloride exhibits significant activity as a modulator of neurotransmitter systems, particularly in the central nervous system (CNS). Early-stage in vitro and in vivo studies suggest its potential in treating neurological disorders such as depression and anxiety. For instance, a 2022 study demonstrated its affinity for serotonin and dopamine receptors, which could explain its observed behavioral effects in animal models.
In addition to its CNS applications, recent research has explored the compound's anti-inflammatory and analgesic properties. A 2023 paper in Bioorganic & Medicinal Chemistry reported that 1-(4-Methylphenyl)cyclobutanamine Hydrochloride inhibits key inflammatory pathways, reducing cytokine production in macrophage cells. These findings open new avenues for its use in chronic inflammatory conditions, though further validation is required.
Despite these promising results, challenges remain in understanding the compound's long-term safety and pharmacokinetic profile. Ongoing studies are investigating its metabolic stability, potential drug-drug interactions, and toxicity. Researchers are also exploring structural derivatives to enhance its efficacy and reduce side effects.
In conclusion, 1-(4-Methylphenyl)cyclobutanamine Hydrochloride (CAS: 1228878-94-1) represents a versatile compound with broad therapeutic potential. Continued research is essential to fully unlock its applications in neurology, inflammation, and beyond. The recent advancements in synthesis and mechanistic understanding underscore its value as a focal point for future drug discovery efforts.
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