Cas no 1214386-12-5 (Methyl 5-chloro-6-methoxypicolinate)
Methyl 5-chloro-6-methoxypicolinate Chemical and Physical Properties
Names and Identifiers
-
- Methyl 5-chloro-6-methoxypicolinate
- methyl 5-chloro-6-methoxypyridine-2-carboxylate
- 1214386-12-5
- SCHEMBL16652958
- Methyl5-chloro-6-methoxypicolinate
- 2-Pyridinecarboxylic acid, 5-chloro-6-methoxy-, methyl ester
-
- Inchi: 1S/C8H8ClNO3/c1-12-7-5(9)3-4-6(10-7)8(11)13-2/h3-4H,1-2H3
- InChI Key: JHMGFCFCTFVGOS-UHFFFAOYSA-N
- SMILES: ClC1C=CC(C(=O)OC)=NC=1OC
Computed Properties
- Exact Mass: 201.0192708g/mol
- Monoisotopic Mass: 201.0192708g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 13
- Rotatable Bond Count: 3
- Complexity: 188
- 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
- Topological Polar Surface Area: 48.4?2
Methyl 5-chloro-6-methoxypicolinate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM178560-1g |
methyl 5-chloro-6-methoxypicolinate |
1214386-12-5 | 95% | 1g |
$489 | 2021-08-05 | |
| Chemenu | CM178560-1g |
methyl 5-chloro-6-methoxypicolinate |
1214386-12-5 | 95% | 1g |
$489 | 2022-06-14 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1604809-1g |
Methyl 5-chloro-6-methoxypicolinate |
1214386-12-5 | 98% | 1g |
¥5953.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1604809-5g |
Methyl 5-chloro-6-methoxypicolinate |
1214386-12-5 | 98% | 5g |
¥11165.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1604809-10g |
Methyl 5-chloro-6-methoxypicolinate |
1214386-12-5 | 98% | 10g |
¥18130.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1604809-25g |
Methyl 5-chloro-6-methoxypicolinate |
1214386-12-5 | 98% | 25g |
¥29595.00 | 2024-08-09 |
Methyl 5-chloro-6-methoxypicolinate Related Literature
-
Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa Caccamo Phys. Chem. Chem. Phys., 2019,21, 11983-11991
-
Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
-
Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
-
Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
-
Xingqun Zheng,Lele Song,Xin Feng,Li Li,Zidong Wei J. Mater. Chem. A, 2020,8, 14145-14151
Additional information on Methyl 5-chloro-6-methoxypicolinate
Recent Advances in the Application of Methyl 5-chloro-6-methoxypicolinate (CAS: 1214386-12-5) in Chemical Biology and Pharmaceutical Research
Methyl 5-chloro-6-methoxypicolinate (CAS: 1214386-12-5) has emerged as a key intermediate in the synthesis of biologically active compounds, particularly in the development of novel pharmaceuticals. Recent studies have highlighted its utility in the construction of heterocyclic scaffolds, which are pivotal in drug discovery. This compound's unique chemical properties, including its reactivity and stability under various conditions, make it an attractive candidate for further exploration in medicinal chemistry.
One of the most significant applications of Methyl 5-chloro-6-methoxypicolinate is in the synthesis of kinase inhibitors. Kinases play a crucial role in cellular signaling pathways, and their dysregulation is associated with numerous diseases, including cancer and inflammatory disorders. Researchers have utilized this compound to develop potent and selective inhibitors targeting specific kinases, demonstrating promising results in preclinical studies. The ability to modify the picolinate moiety allows for fine-tuning of the inhibitors' pharmacokinetic properties, enhancing their therapeutic potential.
In addition to its role in kinase inhibitor development, Methyl 5-chloro-6-methoxypicolinate has been employed in the synthesis of agrochemicals. Its structural features contribute to the efficacy of pesticides and herbicides, offering improved pest control and crop protection. Recent advancements in synthetic methodologies have enabled more efficient and scalable production of this compound, facilitating its broader application in both pharmaceutical and agricultural industries.
Recent publications have also explored the mechanistic insights into the reactivity of Methyl 5-chloro-6-methoxypicolinate. Detailed spectroscopic and computational studies have elucidated its behavior in various chemical transformations, providing a deeper understanding of its potential applications. These findings are instrumental in guiding the design of new derivatives with enhanced biological activity and reduced off-target effects.
Looking ahead, the continued investigation of Methyl 5-chloro-6-methoxypicolinate and its derivatives holds great promise for the discovery of next-generation therapeutics. Collaborative efforts between academic institutions and pharmaceutical companies are expected to accelerate the translation of these findings into clinical applications. The compound's versatility and the growing body of research supporting its use underscore its importance in the field of chemical biology and drug development.
1214386-12-5 (Methyl 5-chloro-6-methoxypicolinate) Related Products
- 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
- 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
- 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
- 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
- 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
- 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
- 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
- 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
- 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
- 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)