Cas no 886574-89-6 (Benzamide, 2-amino-N-methoxy-N,3-dimethyl-)
Benzamide, 2-amino-N-methoxy-N,3-dimethyl- Chemical and Physical Properties
Names and Identifiers
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- Benzamide, 2-amino-N-methoxy-N,3-dimethyl-
- WS-00987
- SCHEMBL5696214
- MFCD12095378
- A1-10026
- CPJXSPMKNKFDQJ-UHFFFAOYSA-N
- CS-0365061
- 2-amino-n-methoxy-n,3-dimethylbenzamide
- D85822
- 886574-89-6
- SY333264
-
- Inchi: 1S/C10H14N2O2/c1-7-5-4-6-8(9(7)11)10(13)12(2)14-3/h4-6H,11H2,1-3H3
- InChI Key: CPJXSPMKNKFDQJ-UHFFFAOYSA-N
- SMILES: O(C)N(C)C(C1C=CC=C(C)C=1N)=O
Computed Properties
- Exact Mass: 194.106
- Monoisotopic Mass: 194.106
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 14
- Rotatable Bond Count: 2
- Complexity: 208
- 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
- Topological Polar Surface Area: 55.6A^2
- XLogP3: 1.7
Benzamide, 2-amino-N-methoxy-N,3-dimethyl- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| eNovation Chemicals LLC | Y1250928-100mg |
2-amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 95% | 100mg |
$185 | 2024-06-05 | |
| eNovation Chemicals LLC | Y1250928-250mg |
2-amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 95% | 250mg |
$310 | 2024-06-05 | |
| eNovation Chemicals LLC | Y1250928-1g |
2-amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 95% | 1g |
$600 | 2024-06-05 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1435731-1g |
2-Amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 98% | 1g |
¥6048.00 | 2024-04-26 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1435731-5g |
2-Amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 98% | 5g |
¥16837.00 | 2024-04-26 | |
| Aaron | AR01JXE2-100mg |
2-amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 95% | 100mg |
$197.00 | 2024-07-18 | |
| Aaron | AR01JXE2-250mg |
2-amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 95% | 250mg |
$356.00 | 2024-07-18 | |
| Aaron | AR01JXE2-500mg |
2-amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 95% | 500mg |
$495.00 | 2024-07-18 | |
| Aaron | AR01JXE2-1g |
2-amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 95% | 1g |
$705.00 | 2024-07-18 | |
| 1PlusChem | 1P01JX5Q-100mg |
2-amino-N-methoxy-N,3-dimethylbenzamide |
886574-89-6 | 95% | 100mg |
$149.00 | 2024-04-20 |
Benzamide, 2-amino-N-methoxy-N,3-dimethyl- Related Literature
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Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
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Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514
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Bo Cao,Yin Wei Chem. Commun., 2018,54, 2870-2873
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M. Sheykhan,S. Khani,S. Shaabanzadeh,M. Joafshan Green Chem., 2017,19, 5940-5948
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Fuming Xiao,Mengzhu Wang,Yunxiang Lei,Wenbo Dai,Yunbing Zhou,Miaochang Liu,Wenxia Gao,Xiaobo Huang,Huayue Wu J. Mater. Chem. C, 2020,8, 17410-17416
Additional information on Benzamide, 2-amino-N-methoxy-N,3-dimethyl-
Benzamide, 2-amino-N-methoxy-N,3-dimethyl- and Its Significance in Modern Chemical Research
The compound with the CAS number 886574-89-6 is a fascinating molecule known as Benzamide, 2-amino-N-methoxy-N,3-dimethyl-. This chemical entity has garnered significant attention in the field of pharmaceutical chemistry due to its unique structural features and potential biological activities. The presence of an amino group at the 2-position, coupled with methoxy and dimethyl substituents on the nitrogen atom, endows this molecule with a distinct chemical profile that makes it a valuable candidate for further investigation.
In recent years, there has been a growing interest in amide-based compounds for their diverse pharmacological properties. Amides are known to exhibit a wide range of biological activities, including anti-inflammatory, analgesic, and anticancer effects. The specific modification of Benzamide, 2-amino-N-methoxy-N,3-dimethyl- not only enhances its solubility but also influences its interaction with biological targets. This has led to extensive research into its potential applications in drug discovery and development.
The structural motif of Benzamide, 2-amino-N-methoxy-N,3-dimethyl- is particularly intriguing because it combines elements that are known to be pharmacologically relevant. The amino group can participate in hydrogen bonding interactions, which are crucial for binding to biological receptors. Meanwhile, the methoxy and dimethyl groups can modulate the electronic properties of the molecule, thereby affecting its binding affinity and selectivity. These features make it an attractive scaffold for designing novel therapeutic agents.
Recent studies have demonstrated that derivatives of benzamide have significant potential in the treatment of various diseases. For instance, some benzamide derivatives have been shown to inhibit the activity of enzymes involved in cancer progression. The compound Benzamide, 2-amino-N-methoxy-N,3-dimethyl-, with its unique substitution pattern, may offer similar benefits. Preliminary in vitro studies suggest that it can interact with specific proteins and enzymes, potentially leading to therapeutic effects.
The synthesis of Benzamide, 2-amino-N-methoxy-N,3-dimethyl- is another area of interest. The development of efficient synthetic routes allows for the production of this compound in larger quantities, which is essential for both research and commercial purposes. Advanced synthetic methodologies have enabled chemists to modify the structure of this molecule further, leading to a library of related compounds that can be screened for biological activity.
In addition to its potential therapeutic applications, Benzamide, 2-amino-N-methoxy-N,3-dimethyl- has also been explored for its role in chemical biology. Researchers are using this compound as a tool to study enzyme mechanisms and protein interactions. By understanding how this molecule interacts with biological targets, scientists can gain insights into disease pathways and develop more effective treatments.
The future prospects for Benzamide, 2-amino-N-methoxy-N,3-dimethyl are promising. Ongoing research aims to uncover new biological activities and optimize its pharmacological properties. Collaborative efforts between chemists and biologists are likely to yield innovative drug candidates based on this scaffold. As our understanding of molecular interactions continues to grow, compounds like Benzamide, 2-amino-N-methoxy-N,3-dimethyl will play an increasingly important role in medicine.
The development of new drugs is a complex process that requires careful consideration of various factors. However, compounds like Benzamide, 2-amino-N-methoxy-N,3-dimethyl offer a starting point for designing molecules with improved efficacy and reduced side effects. By leveraging the unique properties of this compound, researchers can accelerate the discovery of novel therapeutics that address unmet medical needs.
In conclusion, Benzamide, 2-amino-N-methoxy-N,3-dimethyl (CAS number 886574-89-6) is a chemically interesting molecule with significant potential in pharmaceutical research. Its structural features and observed biological activities make it a valuable candidate for further investigation. As research continues to advance,this compound is likely to contribute to the development of new treatments for various diseases.
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