Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504758363 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504758363 |
| Sonrisas canónicas | CCOC(=O)C1=CC(=CC(=N1)C(=O)OCC)Cl |
| IUPAC Name | diethyl 4-chloropyridine-2,6-dicarboxylate |
| InChIKey | XQVRVZXJZVVBLW-UHFFFAOYSA-N |
| INCHI | 1S/C11H12ClNO4/c1-3-16-10(14)8-5-7(12)6-9(13-8)11(15)17-4-2/h5-6H,3-4H2,1-2H3 |
| Isómeros SMILES | CCOC(=O)C1=CC(=CC(=N1)C(=O)OCC)Cl |
| Peso molecular | 257.67 |
| Reaxy-Rn | 219498 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=219498&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Pyridines and derivatives |
| Subclass | Pyridinecarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyridinecarboxylic acids |
| Alternative Parents | Dicarboxylic acids and derivatives Aryl chlorides Heteroaromatic compounds Carboxylic acid esters Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Pyridine carboxylic acid - Aryl chloride - Aryl halide - Dicarboxylic acid or derivatives - Heteroaromatic compound - Carboxylic acid ester - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as pyridinecarboxylic acids. These are compounds containing a pyridine ring bearing a carboxylic acid group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Jun 11, 2026 | D193792 | |
| Certificate of Analysis | Jun 11, 2026 | D193792 | |
| Certificate of Analysis | Jun 11, 2026 | D193792 | |
| Certificate of Analysis | Jun 11, 2026 | D193792 | |
| Certificate of Analysis | Jun 11, 2026 | D193792 | |
| Certificate of Analysis | May 20, 2026 | D193792 | |
| Certificate of Analysis | May 20, 2026 | D193792 | |
| Certificate of Analysis | Aug 07, 2023 | D193792 |
| Peso molecular | 257.670 g/mol |
|---|---|
| XLogP3 | 2.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 6 |
| Exact Mass | 257.045 Da |
| Monoisotopic Mass | 257.045 Da |
| Topological Polar Surface Area | 65.500 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 259.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Shuang Tang, Xue-Lian Hu, Yang-Sen Xu, Wen-Wu Shi, Xin-Zhong Wang, Yu-Xiang Yu, Wei-De Zhang. (2023) Breaking symmetry of carbon nitride skeleton by embedding pyridine ring to promote photocatalytic performance. APPLIED SURFACE SCIENCE, [PMID:] [10.1016/j.apsusc.2023.158921] |