≥99% 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.
2-Chloro-5-nitrobenzoic acid undergoes microwave-assisted, regioselective amination reaction with aliphatic and aromatic amines to yield N-substituted 5-nitroanthranilic acid derivatives. It acts as ligand and forms a red luminescent one dimensional coordination polymer with Eu(III).
| Pubchem Sid | 488182377 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488182377 |
| Sonrisas canónicas | C1=CC(=C(C=C1[N+](=O)[O-])C(=O)O)Cl |
| IUPAC Name | 2-chloro-5-nitrobenzoic acid |
| InChIKey | QUEKGYQTRJVEQC-UHFFFAOYSA-N |
| INCHI | 1S/C7H4ClNO4/c8-6-2-1-4(9(12)13)3-5(6)7(10)11/h1-3H,(H,10,11) |
| Isómeros SMILES | C1=CC(=C(C=C1[N+](=O)[O-])C(=O)O)Cl |
| WGK Alemania | 1 |
| Número ONU | 3077 |
| Peso molecular | 201.56 |
| Beilstein | 1877474 |
| Reaxy-Rn | 1877474 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1877474&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 | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Nitrobenzoic acids and derivatives |
| Alternative Parents | 2-halobenzoic acids Halobenzoic acids Benzoic acids Nitrobenzenes 1-carboxy-2-haloaromatic compounds Benzoyl derivatives Nitroaromatic compounds Chlorobenzenes Aryl chlorides Vinylogous halides Monocarboxylic acids and derivatives Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic oxides Organooxygen compounds Hydrocarbon derivatives Organopnictogen compounds Organochlorides Organonitrogen compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Nitrobenzoate - 2-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - 2-halobenzoic acid - Halobenzoic acid - Benzoic acid - Nitrobenzene - 1-carboxy-2-haloaromatic compound - Nitroaromatic compound - Benzoyl - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Vinylogous halide - Organic nitro compound - C-nitro compound - Carboxylic acid derivative - Carboxylic acid - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organohalogen compound - Organic nitrogen compound - Organochloride - Organonitrogen compound - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as nitrobenzoic acids and derivatives. These are compounds containing a nitrobenzoic acid moiety, which consists of a benzene ring bearing both a carboxylic acid group and a nitro group on two different ring carbon atoms. |
| 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 |
|---|---|---|---|
 I2107115 | Certificate of Analysis | Jun 09, 2025 | C101748 |
| I2107117 | Certificate of Analysis | Jun 09, 2025 | C101748 |
| I2107269 | Certificate of Analysis | Jun 09, 2025 | C101748 |
| F2122050 | Certificate of Analysis | Apr 08, 2025 | C101748 |
| B2528353 | Certificate of Analysis | Jun 18, 2024 | C101748 |
| C2511742 | Certificate of Analysis | Jun 18, 2024 | C101748 |
| C23181000 | Certificate of Analysis | Feb 02, 2023 | C101748 |
| C23181005 | Certificate of Analysis | Feb 02, 2023 | C101748 |
| C23181007 | Certificate of Analysis | Feb 02, 2023 | C101748 |
| C23181009 | Certificate of Analysis | Feb 02, 2023 | C101748 |
| C23181010 | Certificate of Analysis | Feb 02, 2023 | C101748 |
| C1912114 | Certificate of Analysis | Jan 06, 2023 | C101748 |
| Punto de fusión (°C) | 165-168°C |
|---|---|
| Peso molecular | 201.560 g/mol |
| XLogP3 | 2.000 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 200.983 Da |
| Monoisotopic Mass | 200.983 Da |
| Topological Polar Surface Area | 83.100 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 227.000 |
| 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. Zhongyu Zhang, Meng Chen, Mingqiong Tong, Wan Sun, Pingxuan Dong, Xinfeng Song, Xiaoyue Wang. (2022) Syntheses, crystal structure, thermal behavior, and anti-tumor activity of three ternary metal complexes with 2-chloro-5-nitrobenzoic acid and heterocyclic compounds. HETEROCYCLIC COMMUNICATIONS, 28 (1): (84-94). [PMID:] [10.1515/hc-2022-0011] |
