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| | 3,3',5,5'-TETRABROMOBIPHENYL Basic information |
| Product Name: | 3,3',5,5'-TETRABROMOBIPHENYL | | Synonyms: | PBB NO 80;3,3',5,5'-TETRABROMOBIPHENYL;1,3-Dibromo-5-phenylbenzene;3,3',5,5'-Tetrabromobiphenyl, 35μg /mL in Isooctane;pbb 80;3,3',5,5'-Tetrabromo-1,1'-biphenyl;3,5,3',5'-TetrabroMo-biphenyl;1,1'-Biphenyl, 3,3',5,5'-tetrabromo- | | CAS: | 16400-50-3 | | MF: | C12H6Br4 | | MW: | 469.79 | | EINECS: | | | Product Categories: | Aryl;Building Blocks;C9 to C12;Chemical Synthesis;Halogenated Hydrocarbons;Liquid Crystals;Materials Science;Organic and Printed Electronics;Organic Building Blocks | | Mol File: | 16400-50-3.mol |  |
| | 3,3',5,5'-TETRABROMOBIPHENYL Chemical Properties |
| Melting point | 185-190℃ | | Boiling point | 401.8±40.0 °C(Predicted) | | density | 2.140±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Dichloromethane (Slightly) | | form | Solid | | color | White to Off-White | | InChIKey | FXJXZYWFJAXIJX-UHFFFAOYSA-N | | EPA Substance Registry System | 1,1'-Biphenyl, 3,3',5,5'-tetrabromo- (16400-50-3) |
| Hazard Codes | Xi | | Risk Statements | 41 | | Safety Statements | 26-39 | | WGK Germany | 3 |
| | 3,3',5,5'-TETRABROMOBIPHENYL Usage And Synthesis |
| Uses | PBB 80 is a related compound of PBB 37 (P215150), a brominated biphenyls that can be used as a flame retardant and often incorporated into consumer products including appliances, electronics and plastics. | | Uses | 3,3',5,5'-TETRABROMOBIPHENYL can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes. | | Preparation | 1,3,5-tribromobenzene (6.3 g, 20 mmol) was dissolved in diethylether (50 ml). The reaction solution was cooled to -78° C., and n-butyllithium (8.8 ml, 22 mmol, 2.5M in hexane) was gradually added thereto. The reaction mixture was stirred at -78° C. for one hour, and copper chloride (II) (2.96 g, 22 mmol) was added thereto at -78° C. The reaction solution was stirred for five hours and washed with distilled water and ethylacetate at room temperature. The obtained ethylacetate layer was dried over MgSO4, and then dried under a reduced pressure to obtain a crude product. The crude product was purified by silica gel column chromatography to give intermediate A as a white solid (3.74 g, yield: 80%). |
| | 3,3',5,5'-TETRABROMOBIPHENYL Preparation Products And Raw materials |
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