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| | 2,2-dimethylbenzo[1,3]dioxol-4-ol Basic information |
| Product Name: | 2,2-dimethylbenzo[1,3]dioxol-4-ol | | Synonyms: | 1,3-Benzodioxol-4-ol, 2,2-dimethyl-;Bendiocarb phenol;2,2-dimethyl-1,3-benzodioxol-4-ol;2,2-dimethylbenzo[1,3]dioxol-4-ol;2, 2-Dimethyl-4-hydroxy-1,3-benzodioxole;2,2-dimethyl-2H-1,3-benzodioxol-4-ol | | CAS: | 22961-82-6 | | MF: | C9H10O3 | | MW: | 166.17 | | EINECS: | 400-900-7 | | Product Categories: | | | Mol File: | 22961-82-6.mol | ![2,2-dimethylbenzo[1,3]dioxol-4-ol Structure](CAS/GIF/22961-82-6.gif) |
| | 2,2-dimethylbenzo[1,3]dioxol-4-ol Chemical Properties |
| Melting point | 92-93 °C | | Boiling point | 239.6±29.0 °C(Predicted) | | density | 1.208±0.06 g/cm3(Predicted) | | pka | 9.61±0.40(Predicted) | | EPA Substance Registry System | Bendiocarb phenol (22961-82-6) |
| | 2,2-dimethylbenzo[1,3]dioxol-4-ol Usage And Synthesis |
| General Description | White crystalline solid. | | Air & Water Reactions | Hydrolyzes rapidly in alkaline media and decomposes above 125°C. | | Reactivity Profile | 2,2-dimethylbenzo[1,3]dioxol-4-ol is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates. |
| | 2,2-dimethylbenzo[1,3]dioxol-4-ol Preparation Products And Raw materials |
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