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| | 3,4,5-Tribromopyrazole Basic information |
| Product Name: | 3,4,5-Tribromopyrazole | | Synonyms: | 3,4,5-TRIBROMOPYRAZOLE;3,4,5-Tribromopyrazole, 97+%;3,4,5-Tribromopyrazol;3,4,5-TribroMo-1H-pyrazole, 97%, 97%;3,4,5-Tribromo-1H-pyrazoL;1H-Pyrazole, 3,4,5-tribromo-;3,4,5-TRIBROMO-1H-PYRAZOLE | | CAS: | 17635-44-8 | | MF: | C3HBr3N2 | | MW: | 304.77 | | EINECS: | | | Product Categories: | Piperidines;Heterocyclic Compounds;Heterocycles | | Mol File: | 17635-44-8.mol |  |
| | 3,4,5-Tribromopyrazole Chemical Properties |
| Melting point | 190-192°C | | Boiling point | 381.5±37.0 °C(Predicted) | | density | 2.782±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,2-8°C | | solubility | Chloroform, Methanol | | pka | 6.47±0.50(Predicted) | | form | Solid | | color | White to Off-White | | Water Solubility | Insoluble in water. Soluble in Chloroform. | | BRN | 113501 | | InChI | InChI=1S/C3HBr3N2/c4-1-2(5)7-8-3(1)6/h(H,7,8) | | InChIKey | TXQKCKQJBGFUBF-UHFFFAOYSA-N | | SMILES | N1C(Br)=C(Br)C(Br)=N1 | | CAS DataBase Reference | 17635-44-8(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-37 | | RIDADR | UN2811 | | HazardClass | 6.1 | | HS Code | 29331990 |
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ALFA
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| | 3,4,5-Tribromopyrazole Usage And Synthesis |
| Chemical Properties | Off-White Solid | | Uses | 3,4,5-Tribromopyrazole is used in the preparation of 1-aryl-4-substituted piperazine CCR1 antagonists for the treatment of inflammation and immune disorders. | | Uses | 2,4,5-Tribromoimidazole(2,4,5-TBI) on condensation with sugar precursors yields 2,4,5-TBI nucleosides. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. | | Synthesis | Step A: 1H-pyrazole (6.95 g, 0.1 mol) and sodium hydroxide (16 g, 0.4 mol) were dissolved in 400 mL of water, and bromine (48 g, 0.3 mol) was added slowly and dropwise with stirring over 1 hour. The reaction mixture was continued to be stirred for 1 h. The reaction mixture was filtered and the filter cake was washed with deionized water and dried to give 3,4,5-tribromo-1H-pyrazole (25.2 g, 81% yield). Mass spectral analysis showed m/z 302.9 [M + H]+. | | References | [1] Journal of the Chemical Society, Dalton Transactions, 2002, # 11, p. 2297 - 2301
[2] Journal of Medicinal Chemistry, 2016, vol. 59, # 13, p. 6070 - 6085
[3] Patent: US9617268, 2017, B2. Location in patent: Page/Page column 414; 415
[4] Journal of Organic Chemistry, 1986, vol. 51, # 24, p. 4656 - 4660
[5] Tetrahedron, 2007, vol. 63, # 1, p. 56 - 61 |
| | 3,4,5-Tribromopyrazole Preparation Products And Raw materials |
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