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Synonyms
AKOS005259465 | ethyl 2,4-dichloro-5-pyrimidinecarboxylate | SCHEMBL476310 | SY003394 | BBL102625 | 2,4-Dichloro-5-pyrimidine carboxylic acid ethyl ester | Q423975 | BCP21043 | AKOS015838431 | EINECS 257-531-8 | Ethyl2,4-dichloro-5-pyrimidinecarboxylate |
Storage
Store at 2-8°C,Argon charged
Overview Application:
It's employed as an important intermediate for raw material for organic synthesis, agrochemical, pharmaceutical and dyestuff field
Specifications Synonyms
AKOS005259465 | ethyl 2, 4-dichloro-5-pyrimidinecarboxylate | SCHEMBL476310 | SY003394 | BBL102625 | 2, 4-Dichloro-5-pyrimidine carboxylic acid ethyl ester | Q423975 | BCP21043 | AKOS015838431 | EINECS 257-531-8 | Ethyl2, 4-dichloro-5-pyrimidinecarboxylate |
Specifications & Purity
≥98%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 504756554 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504756554 Canonical Smiles CCOC(=O)C1=CN=C(N=C1Cl)Cl IUPAC Name ethyl 2,4-dichloropyrimidine-5-carboxylate InChIKey SRJBDGLSCPDXBL-UHFFFAOYSA-N INCHI 1S/C7H6Cl2N2O2/c1-2-13-6(12)4-3-10-7(9)11-5(4)8/h3H,2H2,1H3 Isomeric SMILES CCOC(=O)C1=CN=C(N=C1Cl)Cl Molecular Weight 221.04 Reaxy-Rn 152173 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=152173&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
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Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Diazines Subclass Pyrimidines and pyrimidine derivatives Intermediate Tree Nodes Pyrimidinecarboxylic acids and derivatives Direct Parent Pyrimidinecarboxylic acids Alternative Parents 2-halopyrimidines Aryl chlorides Vinylogous halides Heteroaromatic compounds Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Pyrimidine-5-carboxylic acid - 2-halopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - Heteroaromatic compound - Vinylogous halide - Carboxylic acid ester - Carboxylic acid derivative - Azacycle - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as pyrimidinecarboxylic acids. These are pyrimidines with a structure containing a carboxyl group attached to the pyrimidine ring. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Certificates(CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in Methanol Sensitivity Moisture Sensitive Flash Point(°C) 142 °C Boil Point(°C) 145 °C/11 mmHg Melt Point(°C) 36 °C Molecular Weight 221.040 g/mol XLogP3 2.300 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 3 Exact Mass 219.981 Da Monoisotopic Mass 219.981 Da Topological Polar Surface Area 52.100 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 191.000 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
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