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| 5-Bromo-2,4-dichloropyrimidine Basic information |
Product Name: | 5-Bromo-2,4-dichloropyrimidine | Synonyms: | BUTTPARK 48\06-22;5-BROMO-2,4-DICHLOROPYRIMIDINE;TIMTEC-BB SBB003301;5-Bromo-2,4-Dichloropyridimidine;5-BROMO-2,4-DICHLOROPYRIMIDINE 99%;2,4-DICHLORO-5-BROMO PYRIMIDINE;5-Bromo-2,4-dichL;5-Bromo-2,4-dichloropyrimidine ,97% | CAS: | 36082-50-5 | MF: | C4HBrCl2N2 | MW: | 227.87 | EINECS: | 629-358-1 | Product Categories: | Building Blocks;C4 to C5;Chemical Synthesis;Halogenated Heterocycles;Heterocyclic Building Blocks;Heterocycle-Pyrimidine series;Pyrimidine Series;pharmacetical;Halides;Pyrazines, Pyrimidines & Pyridazines;Pyrimidine;Heterocyclic Building Blocks;Pyrimidines;PyrimidinesHeterocyclic Building Blocks;Pyridines, Pyrimidines, Purines and Pteredines;Halogenated;Organohalides;Nucleotides and Nucleosides;Aromatics Compounds;Bases & Related Reagents;Nucleotides;Aromatics;Pyrazines, Pyrimidines & Pyridazines;Building Blocks;Halogenated Heterocycles | Mol File: | 36082-50-5.mol | |
| 5-Bromo-2,4-dichloropyrimidine Chemical Properties |
Melting point | 29-30 °C (lit.) | Boiling point | 128 °C/15 mmHg (lit.) | density | 1.781 g/mL at 25 °C (lit.) | refractive index | n20/D 1.603(lit.) | Fp | >230 °F | storage temp. | Inert atmosphere,Room Temperature | solubility | Chloroform (Slightly), Ether (Slightly), Ethyl Acetate (Slightly), Toluene (Slightly) | form | Liquid or Low Melting Solid | pka | -4.26±0.29(Predicted) | Specific Gravity | 1.781 | color | Clear colorless to light yellow | BRN | 124441 | InChIKey | SIKXIUWKPGWBBF-UHFFFAOYSA-N | CAS DataBase Reference | 36082-50-5(CAS DataBase Reference) |
Hazard Codes | T,C | Risk Statements | 23/24/25-34-43 | Safety Statements | 26-27-36/37/39-45 | RIDADR | UN 3263 8/PG 2 | WGK Germany | 3 | Hazard Note | Toxic/Corrosive | HazardClass | 8 | PackingGroup | III | HS Code | 29335990 |
| 5-Bromo-2,4-dichloropyrimidine Usage And Synthesis |
Chemical Properties | Colourless Oil | Uses | Starting material for the synthesis of trisubstituted pyrimidines via a combination of nucleophilic substitution and palladium-catalyzed aryl cross-coupling.1 | Uses | 5-Bromo-2,4-dichloropyrimidine may be employed as starting reagent for the synthesis of positive allosteric modulators for GABAB receptors (drug-like class of compounds) and pyridinepyrimidine analogs. | General Description | 5-Bromo-2,4-dichloropyrimidine is a halogenoprimidine. It has been reported as an intermediate during the synthesis of 2,4-di-t-butoxy-5-bromopyrimidine and 2,4-di-t-butoxy-5-pyrimidineboronic acid. |
| 5-Bromo-2,4-dichloropyrimidine Preparation Products And Raw materials |
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