Cas no 30956-28-6 (2-chloroacetohydrazide)
2-chloroacetohydrazide Chemical and Physical Properties
Names and Identifiers
-
- chloroacetyl hydrazine
- 2-chloroacetohydrazide
- chloroacetic acid hydrazide
- DB-068389
- Acetic acid, 2-chloro-, hydrazide
- chloroacetylhydrazine
- SCHEMBL2957240
- AKOS006383599
- DTXSID60275974
- EN300-331615
- A936073
- VHFJFUOFTHFTNI-UHFFFAOYSA-N
- 30956-28-6
- chloroacetohydrazide
-
- MDL: MFCD19232046
- Inchi: 1S/C2H5ClN2O/c3-1-2(6)5-4/h1,4H2,(H,5,6)
- InChI Key: VHFJFUOFTHFTNI-UHFFFAOYSA-N
- SMILES: ClCC(NN)=O
Computed Properties
- Exact Mass: 108.00915
- Monoisotopic Mass: 108.0090405g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 6
- Rotatable Bond Count: 1
- Complexity: 55.5
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -0.6
- Topological Polar Surface Area: 55.1?2
Experimental Properties
- PSA: 55.12
2-chloroacetohydrazide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-331615-1g |
2-chloroacetohydrazide |
30956-28-6 | 1g |
$1014.0 | 2023-09-04 | ||
| Enamine | EN300-331615-5g |
2-chloroacetohydrazide |
30956-28-6 | 5g |
$2940.0 | 2023-09-04 | ||
| Enamine | EN300-331615-10g |
2-chloroacetohydrazide |
30956-28-6 | 10g |
$4360.0 | 2023-09-04 | ||
| Enamine | EN300-331615-0.05g |
2-chloroacetohydrazide |
30956-28-6 | 0.05g |
$235.0 | 2023-09-04 | ||
| Enamine | EN300-331615-0.1g |
2-chloroacetohydrazide |
30956-28-6 | 0.1g |
$352.0 | 2023-09-04 | ||
| Enamine | EN300-331615-0.25g |
2-chloroacetohydrazide |
30956-28-6 | 0.25g |
$503.0 | 2023-09-04 | ||
| Enamine | EN300-331615-0.5g |
2-chloroacetohydrazide |
30956-28-6 | 0.5g |
$791.0 | 2023-09-04 | ||
| Enamine | EN300-331615-1.0g |
2-chloroacetohydrazide |
30956-28-6 | 1g |
$1014.0 | 2023-06-04 | ||
| Enamine | EN300-331615-2.5g |
2-chloroacetohydrazide |
30956-28-6 | 2.5g |
$1988.0 | 2023-09-04 | ||
| Enamine | EN300-331615-5.0g |
2-chloroacetohydrazide |
30956-28-6 | 5g |
$2940.0 | 2023-06-04 |
2-chloroacetohydrazide Related Literature
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Luis Miguel Azofra,Douglas R. MacFarlane,Chenghua Sun Chem. Commun., 2016,52, 3548-3551
-
Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
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Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580
-
Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
-
Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
Additional information on 2-chloroacetohydrazide
Recent Advances in the Application of 2-Chloroacetohydrazide (CAS: 30956-28-6) in Chemical Biology and Pharmaceutical Research
2-Chloroacetohydrazide (CAS: 30956-28-6) is a versatile chemical compound that has garnered significant attention in recent years due to its potential applications in chemical biology and pharmaceutical research. This hydrazide derivative, characterized by its chloroacetyl functional group, serves as a valuable building block in the synthesis of various bioactive molecules. Recent studies have explored its utility in drug discovery, medicinal chemistry, and chemical biology, highlighting its role as a key intermediate in the development of novel therapeutic agents.
One of the most notable applications of 2-chloroacetohydrazide is its use in the synthesis of hydrazone derivatives, which exhibit a wide range of biological activities. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that hydrazone derivatives synthesized from 2-chloroacetohydrazide displayed potent antimicrobial activity against drug-resistant bacterial strains. The researchers attributed this activity to the compound's ability to disrupt bacterial cell wall synthesis, making it a promising candidate for the development of new antibiotics.
In addition to its antimicrobial properties, 2-chloroacetohydrazide has been investigated for its potential in cancer therapy. A recent study in Bioorganic & Medicinal Chemistry Letters reported the synthesis of a series of 2-chloroacetohydrazide-based compounds that exhibited selective cytotoxicity against cancer cell lines. The study highlighted the compound's ability to induce apoptosis in cancer cells through the inhibition of key signaling pathways, suggesting its potential as a lead compound for anticancer drug development.
Beyond its therapeutic applications, 2-chloroacetohydrazide has also been utilized in chemical biology as a tool for protein modification. A 2022 study in Chemical Communications described the use of 2-chloroacetohydrazide as a reactive handle for the site-specific modification of proteins. The researchers demonstrated that the compound could be used to introduce functional groups onto proteins, enabling the study of protein-protein interactions and the development of protein-based therapeutics.
The synthesis and characterization of 2-chloroacetohydrazide derivatives have also been a focus of recent research. Advanced spectroscopic techniques, such as NMR and mass spectrometry, have been employed to elucidate the structural properties of these derivatives. Furthermore, computational modeling studies have provided insights into the molecular interactions and binding affinities of 2-chloroacetohydrazide-based compounds, aiding in the rational design of more effective drugs.
Despite its promising applications, challenges remain in the optimization of 2-chloroacetohydrazide derivatives for clinical use. Issues such as solubility, stability, and bioavailability need to be addressed to ensure their efficacy and safety in vivo. Ongoing research is focused on overcoming these challenges through structural modifications and formulation strategies.
In conclusion, 2-chloroacetohydrazide (CAS: 30956-28-6) represents a valuable scaffold in chemical biology and pharmaceutical research. Its diverse applications, ranging from antimicrobial and anticancer agents to protein modification tools, underscore its potential in drug discovery and development. Continued research and innovation in this area are expected to yield novel therapeutic agents and advance our understanding of biological systems.
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