Cas no 131002-02-3 (Benzamide, 2-bromo-5-chloro-)
Benzamide, 2-bromo-5-chloro- Chemical and Physical Properties
Names and Identifiers
-
- Benzamide, 2-bromo-5-chloro-
- STL412003
- 2-bromo-5-chlorobenzamide
- 131002-02-3
- SCHEMBL24821886
- DTXSID101312330
- AKOS000297757
-
- Inchi: 1S/C7H5BrClNO/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3H,(H2,10,11)
- InChI Key: MUPYRHASLDDKJT-UHFFFAOYSA-N
- SMILES: C(N)(=O)C1=CC(Cl)=CC=C1Br
Computed Properties
- Exact Mass: 232.92430Da
- Monoisotopic Mass: 232.92430Da
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 11
- Rotatable Bond Count: 1
- Complexity: 165
- 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: 2.1
- Topological Polar Surface Area: 43.1?2
Benzamide, 2-bromo-5-chloro- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A015001684-250mg |
2-Bromo-5-chlorobenzamide |
131002-02-3 | 97% | 250mg |
504.00 USD | 2021-06-21 | |
| Alichem | A015001684-500mg |
2-Bromo-5-chlorobenzamide |
131002-02-3 | 97% | 500mg |
847.60 USD | 2021-06-21 | |
| Alichem | A015001684-1g |
2-Bromo-5-chlorobenzamide |
131002-02-3 | 97% | 1g |
1,549.60 USD | 2021-06-21 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1643176-250mg |
2-Bromo-5-chlorobenzamide |
131002-02-3 | 98% | 250mg |
¥6958.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1643176-500mg |
2-Bromo-5-chlorobenzamide |
131002-02-3 | 98% | 500mg |
¥10029.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1643176-1g |
2-Bromo-5-chlorobenzamide |
131002-02-3 | 98% | 1g |
¥21393.00 | 2024-08-09 |
Benzamide, 2-bromo-5-chloro- Related Literature
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1. An integrated microfluidic 3D tumor system for parallel and high-throughput chemotherapy evaluation?Dan Liu,Rui Hu,Zhongchao Huang,Meilin Sun,Kai Han Analyst, 2020,145, 6447-6455
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Doug Ogrin,Laura H. van Poppel,Simon G. Bott,Andrew R. Barron Dalton Trans., 2004, 3689-3694
-
Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
-
Chandran Rajendran,Govindaswamy Satishkumar,Charlotte Lang,Eric M. Gaigneaux Catal. Sci. Technol., 2020,10, 2583-2592
-
José M. Rivera,Mariana Martín-Hidalgo,Jean C. Rivera-Ríos Org. Biomol. Chem., 2012,10, 7562-7565
Additional information on Benzamide, 2-bromo-5-chloro-
Comprehensive Overview of Benzamide, 2-bromo-5-chloro- (CAS No. 131002-02-3): Properties, Applications, and Industry Insights
Benzamide, 2-bromo-5-chloro- (CAS No. 131002-02-3) is a halogenated aromatic compound widely recognized for its versatile applications in pharmaceutical intermediates, agrochemical synthesis, and material science. With the rising demand for halogenated benzamide derivatives, this compound has garnered significant attention due to its unique molecular structure, characterized by bromine and chlorine substituents at the 2- and 5-positions of the benzamide ring. Researchers and industry professionals frequently search for terms like "2-bromo-5-chlorobenzamide uses" or "CAS 131002-02-3 suppliers," reflecting its commercial and scientific relevance.
The compound's physicochemical properties include a molecular weight of 234.48 g/mol, a crystalline solid form, and moderate solubility in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol. Its stability under controlled conditions makes it suitable for fine chemical synthesis, particularly in the development of bioactive molecules. Recent studies highlight its role as a precursor in the synthesis of antimicrobial agents and herbicides, aligning with global trends in sustainable agriculture and drug discovery.
In the pharmaceutical sector, Benzamide, 2-bromo-5-chloro- is often explored for its potential in kinase inhibitor development, a hot topic in oncology research. Searches for "halogenated benzamides in drug design" have surged, driven by the need for targeted therapies. Additionally, its application in polymer modification and liquid crystal technology addresses growing interest in advanced materials for electronics and optics.
From an industrial perspective, the compound's synthesis typically involves palladium-catalyzed cross-coupling or electrophilic aromatic substitution, methods frequently queried in academic and patent literature. Environmental and regulatory considerations are also critical, with users searching for "green synthesis of 2-bromo-5-chlorobenzamide" to align with green chemistry principles.
In summary, Benzamide, 2-bromo-5-chloro- (CAS No. 131002-02-3) exemplifies the intersection of innovation and practicality, serving as a cornerstone in multiple high-growth industries. Its adaptability to emerging technologies and compliance with sustainability goals ensure its continued prominence in scientific and industrial discourse.
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