ChemicalBook--->CAS DataBase List--->22961-82-6

22961-82-6

22961-82-6 Structure

22961-82-6 Structure
IdentificationBack Directory
[Name]

2,2-dimethylbenzo[1,3]dioxol-4-ol
[CAS]

22961-82-6
[Synonyms]

Bendiocarb phenol
2,2-dimethyl-1,3-benzodioxol-4-ol
2,2-dimethylbenzo[1,3]dioxol-4-ol
1,3-Benzodioxol-4-ol, 2,2-dimethyl-
2,2-dimethyl-2H-1,3-benzodioxol-4-ol
2, 2-Dimethyl-4-hydroxy-1,3-benzodioxole
[EINECS(EC#)]

400-900-7
[Molecular Formula]

C9H10O3
[MOL File]

22961-82-6.mol
[Molecular Weight]

166.17
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

41
[Safety Statements ]

24-26-39
[REACH Registrations]

Inactive
Hazard InformationBack Directory
[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.
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