|  | |  |  | 5-Bromopyrimidine Basic information | 
 | Product Name: | 5-Bromopyrimidine |  | Synonyms: | 5-bromo-pyrimidin;PYRIMIDINE, 2-BROMO-;PYRIMIDINE, 5-BROMO-;5-BROMOPYRIMIDINE;5-Bromopyrimidine,98%;Pyrimidine,5-bromo-(6CI,7CI,8CI,9CI);5-BROMOISATINIC ANHYDRIDE;5-BROMOPYRIMIDINE, 99% MIN |  | CAS: | 4595-59-9 |  | MF: | C4H3BrN2 |  | MW: | 158.98 |  | EINECS: | 224-992-1 |  | Product Categories: | Halides;Pyrazines, Pyrimidines & Pyridazines;Aromatics Compounds;Aromatics;Heterocycles;Pyrazines,  Pyrimidines  &  Pyridazines;HALIDE;Building  Blocks;Halogenated  Heterocycles;Heterocyclic  Building  Blocks;Pyrimidines;PyrimidinesHeterocyclic  Building  Blocks;Pyrimidine;Heterocycle-Pyrimidine series;Pyridines, Pyrimidines, Purines and Pteredines;bc0001;4595-59-9 |  | Mol File: | 4595-59-9.mol |  |  | 
|  |  | 5-Bromopyrimidine Chemical Properties | 
| Hazard Codes | Xi |  | Risk Statements | 36/37/38-36/38 |  | Safety Statements | 26-36-37/39 |  | WGK Germany | 3 |  | Hazard Note | Irritant |  | TSCA | T |  | HazardClass | IRRITANT, KEEP COLD |  | HS Code | 29335990 | 
|  |  | 5-Bromopyrimidine Usage And Synthesis | 
 | Chemical Properties | yellow solid crystalline, insoluble in water, soluble in organic solvents such as benzene and toluene. |  | Uses | 5-Bromopyrimidine was used in the synthesis of N-heteroaryl substituted 9-arylcarbazolyl derivatives via palladium-catalyzed aerobic and ligand-free Suzuki reaction, (5-(phenylethynyl)pyrimidine) via microwave assisted organic synthesis (MAOS) Sonogashira protocol. |  | Uses | 5-Bromopyrimidine was used in the synthesis of: N-heteroaryl substituted 9-arylcarbazolyl derivatives via palladium-catalyzed aerobic and ligand-free Suzuki reaction
 (5-(phenylethynyl)pyrimidine) via microwave assisted organic synthesis (MAOS) Sonogashira protocol
 Intermediate for the synthesis of plant growth regulator flurprimidol
 |  | Application | 5-Bromopyrimidine is a compound useful in organic synthesis. |  | Preparation | 5-Bromopyrimidine is prepared by reacting dibromodifuranone with formamide in the presence of B2O2 catalyst at 180-185°C to obtain the product. |  | General Description | Rapid nucleophilic displacement reactions of 5-bromopyrimidine with nucleophiles under microwave irradiation has been studied. 5-Bromopyrimidine undergoes direct metallation with lithuium diisopropylamide to yield 4-lithio-5-bromopyrimidine. | 
|  |  | 5-Bromopyrimidine Preparation Products And Raw materials | 
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