Cas no 887596-33-0 ((3-bromo-4-methoxyphenyl)methylhydrazine)
(3-bromo-4-methoxyphenyl)methylhydrazine Chemical and Physical Properties
Names and Identifiers
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- 3-BROMO-4-METHOXY-BENZYL-HYDRAZINE
- (3-bromo-4-methoxyphenyl)methylhydrazine
- AKOS000128265
- DTXSID00588196
- [(3-Bromo-4-methoxyphenyl)methyl]hydrazine
- 887596-33-0
- EN300-1260476
-
- MDL: MFCD07786497
- Inchi: 1S/C8H11BrN2O/c1-12-8-3-2-6(5-11-10)4-7(8)9/h2-4,11H,5,10H2,1H3
- InChI Key: MUJQNYGBNJPDPP-UHFFFAOYSA-N
- SMILES: BrC1=C(C=CC(=C1)CNN)OC
Computed Properties
- Exact Mass: 230.00548g/mol
- Monoisotopic Mass: 230.00548g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 12
- Rotatable Bond Count: 3
- Complexity: 134
- 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: 1.2
- Topological Polar Surface Area: 47.3?2
(3-bromo-4-methoxyphenyl)methylhydrazine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1260476-50mg |
[(3-bromo-4-methoxyphenyl)methyl]hydrazine |
887596-33-0 | 50mg |
$348.0 | 2023-10-02 | ||
| Enamine | EN300-1260476-100mg |
[(3-bromo-4-methoxyphenyl)methyl]hydrazine |
887596-33-0 | 100mg |
$364.0 | 2023-10-02 | ||
| Enamine | EN300-1260476-250mg |
[(3-bromo-4-methoxyphenyl)methyl]hydrazine |
887596-33-0 | 250mg |
$381.0 | 2023-10-02 | ||
| Enamine | EN300-1260476-500mg |
[(3-bromo-4-methoxyphenyl)methyl]hydrazine |
887596-33-0 | 500mg |
$397.0 | 2023-10-02 | ||
| Enamine | EN300-1260476-1000mg |
[(3-bromo-4-methoxyphenyl)methyl]hydrazine |
887596-33-0 | 1000mg |
$414.0 | 2023-10-02 | ||
| Enamine | EN300-1260476-2500mg |
[(3-bromo-4-methoxyphenyl)methyl]hydrazine |
887596-33-0 | 2500mg |
$810.0 | 2023-10-02 | ||
| Enamine | EN300-1260476-5000mg |
[(3-bromo-4-methoxyphenyl)methyl]hydrazine |
887596-33-0 | 5000mg |
$1199.0 | 2023-10-02 | ||
| Enamine | EN300-1260476-10000mg |
[(3-bromo-4-methoxyphenyl)methyl]hydrazine |
887596-33-0 | 10000mg |
$1778.0 | 2023-10-02 | ||
| Enamine | EN300-1260476-1.0g |
[(3-bromo-4-methoxyphenyl)methyl]hydrazine |
887596-33-0 | 1g |
$0.0 | 2023-06-08 |
(3-bromo-4-methoxyphenyl)methylhydrazine Related Literature
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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
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Eunhak Lim,Jiyoung Heo,Seong Keun Kim Nanoscale, 2019,11, 11369-11378
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Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
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Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
Additional information on (3-bromo-4-methoxyphenyl)methylhydrazine
Comprehensive Overview of (3-bromo-4-methoxyphenyl)methylhydrazine (CAS No. 887596-33-0): Properties, Applications, and Research Insights
(3-bromo-4-methoxyphenyl)methylhydrazine (CAS No. 887596-33-0) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research due to its unique structural features. The compound belongs to the hydrazine derivatives family, characterized by the presence of a methoxy group and a bromine atom on the phenyl ring. These functional groups contribute to its reactivity and potential applications in drug discovery and material science. Researchers are particularly interested in its role as a building block for synthesizing more complex molecules, given its ability to participate in condensation and coupling reactions.
In recent years, the demand for high-purity intermediates like (3-bromo-4-methoxyphenyl)methylhydrazine has surged, driven by advancements in targeted therapy and precision agriculture. The compound's CAS No. 887596-33-0 is frequently searched in academic databases and chemical supplier platforms, reflecting its relevance in medicinal chemistry. Its brominated aromatic structure makes it a candidate for designing enzyme inhibitors or ligands in catalytic systems. Additionally, the methoxy group enhances solubility, a critical factor in formulation development.
From an environmental perspective, the synthesis and handling of (3-bromo-4-methoxyphenyl)methylhydrazine align with the growing emphasis on green chemistry principles. Laboratories are optimizing protocols to minimize waste and energy consumption during its production. This aligns with broader industry trends, such as the search for sustainable synthetic routes and bio-based alternatives. The compound's stability under controlled conditions also makes it suitable for long-term storage, a key consideration for industrial-scale applications.
Analytical techniques like HPLC and NMR spectroscopy are routinely employed to verify the purity and structural integrity of CAS No. 887596-33-0. These methods ensure compliance with stringent quality control standards, particularly in GMP-certified facilities. The compound's spectral data is often referenced in patent filings, underscoring its proprietary value in intellectual property-driven sectors. Furthermore, its thermal stability has been investigated for potential use in high-performance polymers.
Emerging studies explore the structure-activity relationship (SAR) of (3-bromo-4-methoxyphenyl)methylhydrazine derivatives, particularly in modulating biological pathways. This resonates with the increasing focus on personalized medicine and computational drug design. The compound's molecular weight (253.11 g/mol) and logP value are critical parameters for ADMET profiling, a hot topic in preclinical research. Collaborative efforts between academia and industry continue to uncover novel applications, positioning 887596-33-0 as a versatile tool in chemical biology.
In summary, (3-bromo-4-methoxyphenyl)methylhydrazine represents a compelling case study in the intersection of synthetic chemistry and applied sciences. Its CAS No. 887596-33-0 serves as a gateway to innovations in life sciences and advanced materials. As research methodologies evolve, this compound is poised to play a pivotal role in addressing contemporary challenges, from therapeutic development to environmental sustainability.
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