Molecular Formula | C7H3Cl2NO2 |
Molar Mass | 204.01 |
Density | 1.4521 (rough estimate) |
Melting Point | 56-58 °C (lit.) |
Boling Point | 284 °C (lit.) |
Flash Point | 284°C |
Water Solubility | Insoluble in water. |
Vapor Presure | 0.00292mmHg at 25°C |
Appearance | Crystalline Powder, Crystals or Chunks |
Color | White to brown |
BRN | 131556 |
pKa | -2.12±0.10(Predicted) |
Storage Condition | 2-8℃ |
Sensitive | Moisture Sensitive |
Refractive Index | 1.6100 (estimate) |
MDL | MFCD00006289 |
Use | 2,6-Pyridinedicarbonyl chloride was used as the reagent during the synthesis of pyridine-based polyamido-polyester optically active macrocycles. It was used as starting reagent during the synthesis of pyridine-bridged 2,6-bis-carboxamide Schiff′s bas |
Hazard Symbols | C - Corrosive |
Risk Codes | 34 - Causes burns |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S24/25 - Avoid contact with skin and eyes. |
UN IDs | UN 3261 8/PG 2 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 10-19-21 |
HS Code | 29333990 |
Hazard Class | 8 |
Packing Group | II |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
Application | 2, 6-pyridine dicarbonyl chloride is an organic intermediate and pharmaceutical intermediate that can be used in acylation reactions. It is mainly used in laboratory research and development. In the process of chemical and pharmaceutical research and development, it can be prepared from 2, 6-pyridinedicarboxylic acid and oxalyl chloride. |
preparation | report 1. dissolving 2,6-pyridinedicarboxylic acid (5.00g,30mmol) as raw material in dichloromethane, adding oxalyl chloride (11.43g,90mmol) dropwise at 0 ℃, heating the solution to 25 ℃ after the dropwise addition, stirring the reaction to produce 2,6-pyridinedicarboxylic chloride in a yield of 95%; it is reported that the 2. dissolves 2, 6-pyridinedicarboxylic acid in dichloromethane, then adds a certain amount of dichlorosulfoxide, and refluxes at 70°C to remove the pyridine -2, 6-dicarboxylic acid Two carboxyl acyl chlorides are chlorinated, and finally the impurities produced are removed to prepare 2, 6-pyridine dicarbonyl chloride. |