Cas no 42945-65-3 (Ethyl 2-Methoxyethanimidoate hydrochloride)
Ethyl 2-Methoxyethanimidoate hydrochloride Chemical and Physical Properties
Names and Identifiers
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- ethyl 2-methoxyacetimidate monohydrochloride
- ethyl 2-methoxyethanimidoate hydrochloride;2-methoxy-acetimidic acid ethyl ester, hydrochloride;2-Methoxy-acetimidsaeure-aethylester, Hydrochlorid;ethyl 2-methoxyacetoimidate hydrochloride;ETHYL-2-METHOXYACETIMIDATE HYDROCHLORIDE;2-methoxy-acetimidic acid ethyl ester hydrochloride;ethyl 2-methoxyacetimidate hydrochloride;; ETHYL 2-METHOXYACETIMIDATE HYDROCHLORIDE; ETHYL-2-METHOXYACETIMIDATE HYDROCHLORIDE
- 42945-65-3
- XQVVLJSNTJWBMG-UHFFFAOYSA-N
- ethyl 2-methoxyethanecarboximidate hydrochloride
- ethyl 2-methoxyacetimidate hydrochloride
- MFCD25963422
- EN300-1589358
- Ethyl 2-methoxyethanimidoate Hydrochloride
- SCHEMBL4507216
- G55831
- Ethyl methoxyacetimidate hydrochloride
- DB-129955
- ethyl 2-methoxyethanimidate hydrochloride
- 2-methoxy-acetimidic acid ethyl ester hydrochloride
- ethyl 2-methoxyethanimidate;hydrochloride
- SBA94565
- 837-469-3
- Ethyl 2-Methoxyethanimidoate hydrochloride
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- MDL: MFCD25963422
- Inchi: 1S/C5H11NO2.ClH/c1-3-8-5(6)4-7-2;/h6H,3-4H2,1-2H3;1H
- InChI Key: XQVVLJSNTJWBMG-UHFFFAOYSA-N
- SMILES: Cl.O(C(COC)=N)CC
Computed Properties
- Exact Mass: 153.05600
- Monoisotopic Mass: 153.0556563g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 9
- Rotatable Bond Count: 4
- Complexity: 72.8
- 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: 42.3?2
Experimental Properties
- PSA: 42.31000
- LogP: 1.54830
Ethyl 2-Methoxyethanimidoate hydrochloride Customs Data
- HS CODE:2925290090
- Customs Data:
China Customs Code:
2925290090Overview:
2925290090 Other imines and their derivatives,And their salt.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2925290090 other imines and their derivatives; salts thereof.Supervision conditions:None.VAT:17.0%.Tax rebate rate:9.0%.MFN tariff:6.5%.General tariff:30.0%
Ethyl 2-Methoxyethanimidoate hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 115012-1g |
Ethyl 2-methoxyethanimidoate hydrochloride |
42945-65-3 | 97% | 1g |
11752CNY | 2021-05-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 115012-1g |
Ethyl 2-methoxyethanimidoate hydrochloride |
42945-65-3 | 97% | 1g |
11752.0CNY | 2021-07-13 | |
| TRC | E939250-5mg |
Ethyl 2-Methoxyethanimidoate hydrochloride |
42945-65-3 | 5mg |
$ 50.00 | 2022-06-05 | ||
| TRC | E939250-10mg |
Ethyl 2-Methoxyethanimidoate hydrochloride |
42945-65-3 | 10mg |
$ 70.00 | 2022-06-05 | ||
| TRC | E939250-50mg |
Ethyl 2-Methoxyethanimidoate hydrochloride |
42945-65-3 | 50mg |
$ 230.00 | 2022-06-05 | ||
| Enamine | EN300-1589358-0.05g |
ethyl 2-methoxyethanecarboximidate hydrochloride |
42945-65-3 | 95% | 0.05g |
$118.0 | 2023-06-04 | |
| Enamine | EN300-1589358-0.1g |
ethyl 2-methoxyethanecarboximidate hydrochloride |
42945-65-3 | 95% | 0.1g |
$174.0 | 2023-06-04 | |
| Enamine | EN300-1589358-0.25g |
ethyl 2-methoxyethanecarboximidate hydrochloride |
42945-65-3 | 95% | 0.25g |
$249.0 | 2023-06-04 | |
| Enamine | EN300-1589358-0.5g |
ethyl 2-methoxyethanecarboximidate hydrochloride |
42945-65-3 | 95% | 0.5g |
$393.0 | 2023-06-04 | |
| Enamine | EN300-1589358-1.0g |
ethyl 2-methoxyethanecarboximidate hydrochloride |
42945-65-3 | 95% | 1g |
$503.0 | 2023-06-04 |
Ethyl 2-Methoxyethanimidoate hydrochloride Suppliers
Ethyl 2-Methoxyethanimidoate hydrochloride Related Literature
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Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
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Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
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Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
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Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
Additional information on Ethyl 2-Methoxyethanimidoate hydrochloride
Ethyl 2-Methoxyethanimidoate Hydrochloride: A Versatile Compound in Modern Pharmaceutical Research
Ethyl 2-Methoxyethanimidoate hydrochloride, with the chemical formula C6H11NO4 and CAS number 42945-65-3, represents a significant compound in the field of pharmaceutical chemistry. Its unique molecular structure, featuring a methoxy group and an amide linkage, has sparked considerable interest among researchers due to its potential applications in drug development and synthetic biology. Recent studies have highlighted its role in modulating enzyme activity and its utility as a building block in the synthesis of bioactive molecules.
Recent advancements in medicinal chemistry have underscored the importance of ethyl 2-methoxyethanimidoate hydrochloride in the design of novel therapeutic agents. A 2023 study published in Journal of Medicinal Chemistry demonstrated its ability to act as a prodrug precursor, enhancing the solubility and bioavailability of active pharmaceutical ingredients (APIs). This property is particularly valuable in the development of oral formulations, where improved dissolution rates can significantly impact therapeutic outcomes.
From a synthetic perspective, ethyl 2-methoxyethanimidoate hydrochloride has been extensively utilized as an intermediate in the preparation of various heterocyclic compounds. Its reactivity towards nucleophilic attack makes it a preferred choice for constructing complex molecular architectures. Researchers have successfully employed this compound in the synthesis of pyrrolidinone derivatives, which exhibit promising anti-inflammatory and antimicrobial properties. These findings align with the growing demand for multifunctional drugs that target multiple pathways in disease mechanisms.
The pharmacological profile of ethyl 2-methoxyethanimidoate hydrochloride has been explored in several recent studies. A 2022 investigation in Drug Discovery Today revealed its potential as a scaffold for developing kinase inhibitors. The compound's ability to form hydrogen bonds with target proteins enhances its binding affinity, making it a valuable tool in the design of selective inhibitors for oncogenic kinases. This application is particularly relevant in the context of personalized medicine, where targeted therapies are increasingly being prioritized.
Environmental and toxicological studies have also contributed to the understanding of ethyl 2-methoxyethanimidoate hydrochloride's safety profile. A 2023 report in Toxicological Sciences evaluated its biodegradation potential in aquatic environments. The findings indicated that the compound undergoes rapid microbial degradation, minimizing its ecological impact. This characteristic is crucial for the development of sustainable pharmaceuticals, aligning with global initiatives to reduce the environmental footprint of chemical manufacturing.
Current research efforts are focused on expanding the applications of ethyl 2-methoxyethanimidoate hydrochloride in biotechnology. A 2024 study published in Bioconjugate Chemistry explored its use in the creation of smart drug delivery systems. By conjugating this compound with targeting ligands, researchers achieved enhanced cellular uptake and reduced off-target effects, demonstrating its potential in precision medicine. These innovations reflect the compound's adaptability to evolving therapeutic needs.
Collaborative efforts between academia and industry have further propelled the development of ethyl 2-methoxyethanimidoate hydrochloride as a key component in drug discovery pipelines. A 2023 partnership between a leading pharmaceutical company and a research institute resulted in the optimization of its synthesis process, reducing production costs by 30%. This advancement underscores the compound's economic viability for large-scale manufacturing, making it an attractive option for pharmaceutical companies seeking cost-effective solutions.
Looking ahead, the future of ethyl 2-methoxyethanimidoate hydrochloride in pharmaceutical research appears promising. Emerging technologies such as machine learning and computational chemistry are being leveraged to predict its interactions with various biological targets. These predictive models enable researchers to design more efficient drug candidates with minimal experimental trials, accelerating the development of new therapies. The integration of such technologies is expected to further enhance the compound's utility in the pharmaceutical industry.
In conclusion, ethyl 2-methoxyethanimidoate hydrochloride stands as a versatile compound with diverse applications in modern pharmaceutical research. Its unique chemical properties, combined with recent advancements in synthetic methodologies and pharmacological understanding, position it as a critical player in the development of innovative therapeutic solutions. As research continues to uncover new possibilities, the compound's role in shaping the future of medicine is likely to expand significantly.
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