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| 1,1,3,3-TETRABROMOACETONE Basic information |
Product Name: | 1,1,3,3-TETRABROMOACETONE | Synonyms: | 1,1,3,3-TETRABROMOACETONE 95+%;1,1,3,3-tetrabroMopropan-2-one;1,1,3,3-Tetrabromopropanone;1,1,3,3-TETRABROMO-2-PROPANONE;1,1,3,3-TETRABROMOACETONE;Tetrabromoacetone;alpha,alpha,alpha',alpha'-Tetrabromoacetone;2-Propanone, 1,1,3,3-tetrabromo- | CAS: | 22612-89-1 | MF: | C3H2Br4O | MW: | 373.66 | EINECS: | | Product Categories: | Carbonyl Compounds;Halides | Mol File: | 22612-89-1.mol | |
| 1,1,3,3-TETRABROMOACETONE Chemical Properties |
Melting point | 36°C | Boiling point | 129-130 °C(Press: 7 Torr) | density | 2.904±0.06 g/cm3(Predicted) | storage temp. | Refrigerator | solubility | Chloroform, Dichloromethane, Ethyl Acetate, Methanol | form | Solid | color | White Low Melting | Stability: | Temperature Sensitive | InChIKey | SAMNBOHOBWEEEU-UHFFFAOYSA-N |
| 1,1,3,3-TETRABROMOACETONE Usage And Synthesis |
Uses | 1,1,3,3-Tetrabromoacetone is an intermediate in the synthesis of 3-Chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone-13C5, which is an isotope labelled Mutagen X (MX) is a chlorinated furanone that accounts for more of the mutagenic activity of drinking water than any other disinfection byproduct. DNA damages provoked by the six mutagens (furylframide, MX, 4-nitroquinoline N-oxide, sodium azide, 1-nitropyrene, and captan) used in the present study have been known to subject to the nucleotide excision repair system. |
| 1,1,3,3-TETRABROMOACETONE Preparation Products And Raw materials |
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