Cas no 1305711-44-7 (5-Bromo-2,4-dichlorobenzamide)
5-Bromo-2,4-dichlorobenzamide Chemical and Physical Properties
Names and Identifiers
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- 5-Bromo-2,4-dichlorobenzamide
- Benzamide, 5-bromo-2,4-dichloro-
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- MDL: MFCD13191324
- Inchi: 1S/C7H4BrCl2NO/c8-4-1-3(7(11)12)5(9)2-6(4)10/h1-2H,(H2,11,12)
- InChI Key: OJXBLEGDYNPHQP-UHFFFAOYSA-N
- SMILES: C(N)(=O)C1=CC(Br)=C(Cl)C=C1Cl
5-Bromo-2,4-dichlorobenzamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB418797-1 g |
5-Bromo-2,4-dichlorobenzamide |
1305711-44-7 | 1g |
€275.90 | 2023-04-24 | ||
| Apollo Scientific | OR110487-1g |
5-Bromo-2,4-dichlorobenzamide |
1305711-44-7 | 1g |
£202.00 | 2023-09-01 | ||
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD602867-1g |
5-Bromo-2,4-dichlorobenzamide |
1305711-44-7 | 97% | 1g |
¥2002.0 | 2023-04-03 | |
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD602867-5g |
5-Bromo-2,4-dichlorobenzamide |
1305711-44-7 | 97% | 5g |
¥5992.0 | 2023-04-03 | |
| Fluorochem | 518445-1g |
5-bromo-2,4-dichlorobenzamide |
1305711-44-7 | 1g |
£221.00 | 2023-04-20 | ||
| abcr | AB418797-1g |
5-Bromo-2,4-dichlorobenzamide; . |
1305711-44-7 | 1g |
€271.40 | 2024-04-19 | ||
| Ambeed | A775880-1g |
5-Bromo-2,4-dichlorobenzamide |
1305711-44-7 | 97% | 1g |
$291.0 | 2024-04-24 | |
| Ambeed | A775880-5g |
5-Bromo-2,4-dichlorobenzamide |
1305711-44-7 | 97% | 5g |
$873.0 | 2024-04-24 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1515040-50mg |
5-Bromo-2,4-dichlorobenzamide |
1305711-44-7 | 98% | 50mg |
¥1392.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1515040-100mg |
5-Bromo-2,4-dichlorobenzamide |
1305711-44-7 | 98% | 100mg |
¥2002.00 | 2024-08-09 |
5-Bromo-2,4-dichlorobenzamide Related Literature
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Chongyang Zhu,Xiaojia Bian,Xin Jia,Ning Tang,Yongqiang Cheng Food Funct., 2020,11, 10635-10644
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Xue-Ying Wang,Ying Pei,Min Xie,Zi-He Jin,Ya-Shi Xiao,Yang Wang,Li-Na Zhang,Yan Li,Wei-Hua Huang Lab Chip, 2015,15, 1178-1187
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Bidyut Kumar Kundu,Rinky Singh,Ritudhwaj Tiwari,Debasis Nayak New J. Chem., 2019,43, 4867-4877
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Bidou Wang,Xifeng Chen Analyst, 2014,139, 5695-5699
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Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
Additional information on 5-Bromo-2,4-dichlorobenzamide
Introduction to 5-Bromo-2,4-dichlorobenzamide (CAS No. 1305711-44-7)
5-Bromo-2,4-dichlorobenzamide, identified by its Chemical Abstracts Service (CAS) number 1305711-44-7, is a specialized organic compound that has garnered significant attention in the field of pharmaceutical and agrochemical research. This compound belongs to the class of benzamide derivatives, characterized by its bromine and chlorine substituents, which contribute to its unique chemical properties and reactivity. The structural framework of 5-Bromo-2,4-dichlorobenzamide makes it a versatile intermediate in synthetic chemistry, particularly in the development of novel bioactive molecules.
The significance of 5-Bromo-2,4-dichlorobenzamide lies in its potential applications across multiple domains, including medicinal chemistry and material science. Its molecular structure, featuring both bromine and chlorine atoms at specific positions, enhances its utility as a building block for more complex compounds. In recent years, there has been a growing interest in exploring the pharmacological properties of benzamide derivatives due to their demonstrated efficacy in various biological assays.
One of the most compelling aspects of 5-Bromo-2,4-dichlorobenzamide is its role in the synthesis of bioactive molecules. Researchers have leveraged its reactive sites to develop compounds with potential therapeutic applications. For instance, studies have indicated that derivatives of this molecule exhibit inhibitory effects on certain enzymes and receptors, making them candidates for further investigation in drug discovery programs. The bromine and chlorine substituents are particularly noteworthy, as they can be selectively modified through various chemical reactions to tailor the properties of the resulting compounds.
In the realm of medicinal chemistry, 5-Bromo-2,4-dichlorobenzamide has been utilized as a precursor in the synthesis of novel antimicrobial agents. The presence of halogen atoms in its structure facilitates cross-coupling reactions, which are essential for constructing more intricate molecular architectures. These reactions often involve palladium catalysts and are widely employed in the preparation of complex organic molecules. The ability to introduce functional groups at specific positions on the benzamide core allows for fine-tuning of biological activity.
Recent advancements in computational chemistry have further enhanced the understanding of 5-Bromo-2,4-dichlorobenzamide's reactivity and potential applications. Molecular modeling studies have revealed insights into how this compound interacts with biological targets, providing a foundation for rational drug design. By integrating experimental data with computational predictions, researchers can optimize synthetic pathways and improve the efficiency of drug development processes.
The agrochemical industry has also shown interest in 5-Bromo-2,4-dichlorobenzamide, recognizing its potential as a precursor for herbicides and pesticides. The structural features of this compound contribute to its ability to disrupt metabolic pathways in pests, offering a promising avenue for developing environmentally sustainable solutions. Additionally, its stability under various environmental conditions makes it a suitable candidate for field applications.
From a synthetic chemistry perspective, 5-Bromo-2,4-dichlorobenzamide serves as an excellent scaffold for exploring new reaction methodologies. Its versatility allows chemists to employ a wide range of synthetic strategies, including nucleophilic aromatic substitution and metal-catalyzed coupling reactions. These approaches have enabled the preparation of diverse derivatives with tailored properties, expanding the chemical space available for drug discovery and material science applications.
The development of novel synthetic routes for 5-Bromo-2,4-dichlorobenzamide has been accompanied by improvements in green chemistry principles. Efforts have been made to minimize waste and reduce energy consumption during synthesis, aligning with global initiatives to promote sustainable practices. Such advancements not only enhance the efficiency of chemical production but also contribute to environmental conservation.
In conclusion, 5-Bromo-2,4-dichlorobenzamide (CAS No. 1305711-44-7) is a multifaceted compound with significant potential in pharmaceuticals and agrochemicals. Its unique structural features enable diverse applications across multiple research areas, from drug discovery to sustainable agriculture. As scientific understanding continues to evolve, further exploration of this molecule is expected to yield innovative solutions and advancements.
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