Cas no 1955554-26-3 (3-cyclobutylmorpholine hydrochloride)
3-cyclobutylmorpholine hydrochloride Chemical and Physical Properties
Names and Identifiers
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- Morpholine, 3-cyclobutyl-, hydrochloride
- 3-cyclobutylmorpholine hydrochloride
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- MDL: MFCD29036961
- Inchi: 1S/C8H15NO.ClH/c1-2-7(3-1)8-6-10-5-4-9-8;/h7-9H,1-6H2;1H
- InChI Key: YHJGXENKOAGJES-UHFFFAOYSA-N
- SMILES: C1(C2NCCOC2)CCC1.Cl
3-cyclobutylmorpholine hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-262746-0.05g |
3-cyclobutylmorpholine hydrochloride |
1955554-26-3 | 95% | 0.05g |
$794.0 | 2024-06-18 | |
| Enamine | EN300-262746-0.1g |
3-cyclobutylmorpholine hydrochloride |
1955554-26-3 | 95% | 0.1g |
$832.0 | 2024-06-18 | |
| Enamine | EN300-262746-0.25g |
3-cyclobutylmorpholine hydrochloride |
1955554-26-3 | 95% | 0.25g |
$869.0 | 2024-06-18 | |
| Enamine | EN300-262746-0.5g |
3-cyclobutylmorpholine hydrochloride |
1955554-26-3 | 95% | 0.5g |
$907.0 | 2024-06-18 | |
| Enamine | EN300-262746-1.0g |
3-cyclobutylmorpholine hydrochloride |
1955554-26-3 | 95% | 1.0g |
$945.0 | 2024-06-18 | |
| Enamine | EN300-262746-2.5g |
3-cyclobutylmorpholine hydrochloride |
1955554-26-3 | 95% | 2.5g |
$1984.0 | 2024-06-18 | |
| Enamine | EN300-262746-5.0g |
3-cyclobutylmorpholine hydrochloride |
1955554-26-3 | 95% | 5.0g |
$3922.0 | 2024-06-18 | |
| Enamine | EN300-262746-10.0g |
3-cyclobutylmorpholine hydrochloride |
1955554-26-3 | 95% | 10.0g |
$7654.0 | 2024-06-18 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1576019-250mg |
3-Cyclobutylmorpholine hydrochloride |
1955554-26-3 | 98% | 250mg |
¥9198 | 2023-03-01 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1576019-500mg |
3-Cyclobutylmorpholine hydrochloride |
1955554-26-3 | 98% | 500mg |
¥18387 | 2023-03-01 |
3-cyclobutylmorpholine hydrochloride Related Literature
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Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
Additional information on 3-cyclobutylmorpholine hydrochloride
3-Cyclobutylmorpholine Hydrochloride: A Comprehensive Overview
The compound 3-cyclobutylmorpholine hydrochloride (CAS No. 1955554-26-3) is a fascinating molecule with significant potential in various fields, particularly in pharmaceutical and chemical research. This compound belongs to the class of morpholines, which are six-membered heterocyclic amines. The presence of a cyclobutyl group at the third position of the morpholine ring introduces unique structural and functional properties, making it a subject of interest for researchers and industry professionals alike.
Morpholines are widely recognized for their versatility in organic synthesis and their ability to act as building blocks for more complex molecules. The cyclobutyl group, a four-membered ring with significant ring strain, adds an additional layer of complexity to the molecule. This combination of structural features makes 3-cyclobutylmorpholine hydrochloride a valuable compound for exploring novel chemical reactions and drug design strategies.
Recent studies have highlighted the potential of 3-cyclobutylmorpholine hydrochloride in medicinal chemistry. Its ability to form stable hydrogen bonds and its unique electronic properties make it an ideal candidate for drug delivery systems. Researchers have also explored its role as a precursor in the synthesis of bioactive compounds, particularly in the development of anti-inflammatory and antiviral agents.
The synthesis of 3-cyclobutylmorpholine hydrochloride involves a multi-step process that typically begins with the preparation of cyclobutylamine derivatives. The subsequent reaction with morpholine derivatives under specific conditions leads to the formation of the desired product. This process requires precise control over reaction conditions, including temperature and pH, to ensure high yield and purity.
One of the most intriguing aspects of 3-cyclobutylmorpholine hydrochloride is its ability to undergo various transformations under different reaction conditions. For instance, it can participate in nucleophilic substitutions, additions, and eliminations, making it a versatile starting material for organic synthesis. Recent advancements in catalytic methods have further expanded its applicability in asymmetric synthesis and enantioselective reactions.
In terms of pharmacological applications, 3-cyclobutylmorpholine hydrochloride has shown promise as a lead compound for developing new drugs. Its ability to modulate cellular pathways involved in inflammation and viral replication has been extensively studied. Preclinical studies suggest that it may possess anti-inflammatory properties comparable to existing drugs but with potentially fewer side effects.
Moreover, the compound's stability under physiological conditions makes it an attractive candidate for drug delivery systems. Researchers have explored its use as a carrier for delivering therapeutic agents across biological membranes. Its ability to form stable complexes with other molecules further enhances its potential in this area.
From an environmental standpoint, 3-cyclobutylmorpholine hydrochloride exhibits favorable biodegradation properties, making it less likely to accumulate in ecosystems. This characteristic aligns with current trends toward sustainable chemistry and green pharmaceutical development.
In conclusion, 3-cyclobutylmorpholine hydrochloride (CAS No. 1955554-26-3) is a multifaceted compound with significant potential across various domains. Its unique structural features, versatile reactivity, and promising pharmacological properties make it a valuable addition to both academic research and industrial applications. As ongoing studies continue to uncover new insights into its capabilities, this compound is poised to play an increasingly important role in the development of innovative solutions in chemistry and medicine.
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