Cas no 141244-86-2 (2-(2,4-Dibromophenoxy)acetohydrazide)
2-(2,4-Dibromophenoxy)acetohydrazide Chemical and Physical Properties
Names and Identifiers
-
- 2-(2,4-Dibromophenoxy)acetohydrazide
- ALBB-002750
- SR-01000636450-1
- MFCD00098698
- 141244-86-2
- NSC-618810
- AB00083127-01
- DTXSID20326855
- VS-04255
- CS-0316483
- STK036070
- NSC618810
- SB86082
- BBL014288
- CCG-46776
- AKOS000305737
- (2,4-DIBROMO-PHENOXY)-ACETIC ACID HYDRAZIDE
-
- MDL: MFCD00098698
- Inchi: 1S/C8H8Br2N2O2/c9-5-1-2-7(6(10)3-5)14-4-8(13)12-11/h1-3H,4,11H2,(H,12,13)
- InChI Key: ZLCWJMAWCQNODX-UHFFFAOYSA-N
- SMILES: BrC1C=C(C=CC=1OCC(NN)=O)Br
Computed Properties
- Exact Mass: 323.89320g/mol
- Monoisotopic Mass: 321.89525g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 14
- Rotatable Bond Count: 4
- Complexity: 204
- 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: 1.9
- Topological Polar Surface Area: 64.4?2
Experimental Properties
- Density: 1.9±0.1 g/cm3
- Boiling Point: 481.3±35.0 °C at 760 mmHg
- Flash Point: 244.9±25.9 °C
- Vapor Pressure: 0.0±1.2 mmHg at 25°C
2-(2,4-Dibromophenoxy)acetohydrazide Security Information
- Signal Word:warning
- Hazard Statement: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
-
Hazardous Material Identification:
- HazardClass:IRRITANT
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
2-(2,4-Dibromophenoxy)acetohydrazide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B426995-100mg |
2-(2,4-dibromophenoxy)acetohydrazide |
141244-86-2 | 100mg |
$ 70.00 | 2022-06-07 | ||
| TRC | B426995-500mg |
2-(2,4-dibromophenoxy)acetohydrazide |
141244-86-2 | 500mg |
$ 230.00 | 2022-06-07 | ||
| TRC | B426995-1g |
2-(2,4-dibromophenoxy)acetohydrazide |
141244-86-2 | 1g |
$ 340.00 | 2022-06-07 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 023984-500mg |
2-(2,4-Dibromophenoxy)acetohydrazide |
141244-86-2 | 500mg |
1608CNY | 2021-05-07 | ||
| abcr | AB378358-500 mg |
2-(2,4-Dibromophenoxy)acetohydrazide |
141244-86-2 | 500MG |
€195.40 | 2023-02-20 | ||
| abcr | AB378358-1 g |
2-(2,4-Dibromophenoxy)acetohydrazide |
141244-86-2 | 1 g |
€239.00 | 2023-07-19 | ||
| abcr | AB378358-5 g |
2-(2,4-Dibromophenoxy)acetohydrazide |
141244-86-2 | 5 g |
€656.50 | 2023-07-19 | ||
| abcr | AB378358-10 g |
2-(2,4-Dibromophenoxy)acetohydrazide |
141244-86-2 | 10 g |
€1,074.00 | 2023-07-19 | ||
| Chemenu | CM114362-5g |
2-(2,4-dibromophenoxy)acetohydrazide |
141244-86-2 | 95% | 5g |
$420 | 2023-02-18 | |
| Chemenu | CM114362-10g |
2-(2,4-dibromophenoxy)acetohydrazide |
141244-86-2 | 95% | 10g |
$720 | 2023-02-18 |
2-(2,4-Dibromophenoxy)acetohydrazide Related Literature
-
Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
-
Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
-
Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
-
Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
-
Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
Additional information on 2-(2,4-Dibromophenoxy)acetohydrazide
Recent Advances in the Study of 2-(2,4-Dibromophenoxy)acetohydrazide (CAS: 141244-86-2) in Chemical Biology and Pharmaceutical Research
The compound 2-(2,4-Dibromophenoxy)acetohydrazide (CAS: 141244-86-2) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential applications in drug discovery and development. This hydrazide derivative, characterized by its unique bromophenoxy moiety, has been the subject of several studies aimed at elucidating its biological activities, mechanisms of action, and potential therapeutic uses. The following sections provide a comprehensive overview of the latest research findings related to this compound, highlighting its significance in contemporary scientific investigations.
Recent studies have focused on the synthesis and structural optimization of 2-(2,4-Dibromophenoxy)acetohydrazide to enhance its pharmacological properties. Researchers have employed advanced synthetic techniques, including microwave-assisted synthesis and green chemistry approaches, to improve yield and purity. Structural modifications, such as the introduction of additional functional groups, have been explored to increase the compound's bioavailability and target specificity. These efforts have yielded promising results, with several derivatives demonstrating enhanced activity in preliminary biological assays.
In vitro and in vivo studies have revealed that 2-(2,4-Dibromophenoxy)acetohydrazide exhibits notable antimicrobial and anticancer properties. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated that the compound effectively inhibits the growth of multidrug-resistant bacterial strains, including methicillin-resistant Staphylococcus aureus (MRSA). The mechanism of action appears to involve disruption of bacterial cell membrane integrity and inhibition of key enzymatic pathways. Additionally, the compound has shown cytotoxic effects against various cancer cell lines, with particular efficacy observed in breast and lung cancer models. These findings suggest its potential as a lead compound for the development of novel antimicrobial and anticancer agents.
Further investigations into the molecular mechanisms underlying the biological activities of 2-(2,4-Dibromophenoxy)acetohydrazide have employed computational modeling and high-throughput screening techniques. Molecular docking studies have identified potential binding interactions with bacterial DNA gyrase and human topoisomerase II, providing insights into its dual antimicrobial and anticancer effects. Moreover, transcriptomic and proteomic analyses have revealed that the compound modulates the expression of genes involved in oxidative stress response and apoptosis, further elucidating its multifaceted pharmacological profile.
Despite these promising findings, challenges remain in the clinical translation of 2-(2,4-Dibromophenoxy)acetohydrazide. Issues such as solubility, stability, and potential toxicity need to be addressed through further preclinical studies. Recent efforts have focused on formulating the compound into nanoparticle-based delivery systems to enhance its pharmacokinetic properties. Preliminary results from animal studies indicate that such formulations can improve bioavailability and reduce off-target effects, paving the way for future clinical trials.
In conclusion, 2-(2,4-Dibromophenoxy)acetohydrazide (CAS: 141244-86-2) represents a promising candidate for drug development, with demonstrated antimicrobial and anticancer activities. Ongoing research aims to optimize its chemical structure, elucidate its mechanisms of action, and overcome translational challenges. The compound's unique properties and versatile applications underscore its potential to contribute significantly to the advancement of chemical biology and pharmaceutical science.
141244-86-2 (2-(2,4-Dibromophenoxy)acetohydrazide) Related Products
- 5402-32-4(2-(2-bromophenoxy)propanehydrazide)
- 315248-38-5(2-(1-Bromo-2-naphthyl)oxyacetohydrazide)
- 328085-17-2(2-(2-Bromophenoxy)acetohydrazide)
- 16738-00-4(2-(4-Bromophenoxy)acetohydrazide)
- 356100-06-6(2-(2,4-Dibromo-6-methylphenoxy)acetohydrazide)
- 327070-44-0(2-(4-Bromo-3-methylphenoxy)acetohydrazide)
- 6079-89-6(Octadecanoic acid,2,2-dimethylhydrazide)
- 52570-06-6(2-(2-Bromo-4-tert-butylphenoxy)acetohydrazide)
- 308292-49-1(2-(3-Bromophenoxy)acetohydrazide)
- 438219-93-3(2-(6-Bromo-2-naphthyl)oxyacetohydrazide)