| Identification | Back Directory | [Name]
METHYL 2,4-DICHLOROPYRIMIDINE-6-CARBOXYLATE | [CAS]
16492-28-7 | [Synonyms]
NSC46804
2,6-Dichloropyrimidine-4-carboxylicaci
2,6-DichloropyriMidin-4-carboxylic acid
2,4-Dichloropyrimidine-6-carboxylic acid
2,6-DICHLORO-PYRIMIDINE-4-CARBOXYLIC ACID
2,6-DICHLORO-4-PYRIMIDINE CARBOXYLIC ACID
4-PyriMidinecarboxylic acid, 2,6-dichloro-
Methyl 2,6-dichloro-4-pyrimidinecarboxylate
2,6-DICHLOROPYRIMIDINE-4-CARBOXYLIC ACID,97%
2,6-DICHLORO-4-PYRIMIDINE CARBOXYLIC ACID METHYL ESTER | [Molecular Formula]
C5H2Cl2N2O2 | [MDL Number]
MFCD01941317 | [MOL File]
16492-28-7.mol | [Molecular Weight]
192.99 |
| Chemical Properties | Back Directory | [Melting point ]
54-56°C | [Boiling point ]
374.9±22.0 °C(Predicted) | [density ]
1.718±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C, stored under nitrogen | [pka]
2.07±0.10(Predicted) | [Appearance]
Light yellow to yellow Solid | [Water Solubility ]
Slightly soluble in water. | [InChI]
1S/C5H2Cl2N2O2/c6-3-1-2(4(10)11)8-5(7)9-3/h1H,(H,10,11) | [InChIKey]
MOXUTXQEKYPKKS-UHFFFAOYSA-N | [SMILES]
OC(=O)c1cc(Cl)nc(Cl)n1 |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
36/38 | [Safety Statements ]
26 | [WGK Germany ]
3 | [HazardClass ]
IRRITANT, KEEP COLD | [HS Code ]
29335990 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2 |
| Hazard Information | Back Directory | [Uses]
2,6-Dichloropyrimidine-4-carboxylic acid is used as pharmaceutical intermediate. | [General Description]
2,6-Dichloropyrimidine-4-carboxylic acid is a chloropyrimidine compound. Its pyrimidine ring bears two reactive functional groups—chlorine atoms—and a carboxyl group. In the presence of methanol, the chlorine atoms at positions 2 and 6 undergo solvolysis to form hydroxyl groups; hydrolysis in boiling water yields uracil. This substance is highly reactive and can serve as an intermediate in the synthesis of other chloropyrimidines[1].
| [References]
[1] Rand, L., Swisher, J. V., Cronin, C. J. (1962). Reactions Catalyzed by Potassium Fluoride. III. The Knoevenagel Reaction. The Journal of Organic Chemistry, 27 10, 3505–3507. https://doi.org/10.1021/jo01057a024 |
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