2,3-Dihydro-2,2-dimethyl-7-benzofuranol
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2,3-Dihydro-2,2-dimethyl-7-benzofuranol ??
- ?? ?
- 95°C 1mm
- ??
- 1.101 g/mL at 25 °C (lit.)
- ???
- n
20/D 1.541(lit.)
- ???
- >230 °F
- ?? ??
- 2-8°C
- ???
- ?????(?? ???), ???(?? ???)
- ??? ??
- ??
- ?? ?? (pKa)
- 10.10±0.40(Predicted)
- Specific Gravity
- 1.101
- ??
- ??
- CAS ??????
- 1563-38-8(CAS DataBase Reference)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
??? ?? | Xi | ||
---|---|---|---|
?? ???? ?? | 36/37/38 | ||
????? | 26-37/39 | ||
????(UN No.) | UN 3082 9 / PGIII | ||
WGK ?? | 3 | ||
RTECS ?? | DF7708985 | ||
HS ?? | 2932990090 | ||
?? ?? ??? | 1563-38-8(Hazardous Substances Data) | ||
???? ?? | KE-10617 |
2,3-Dihydro-2,2-dimethyl-7-benzofuranol C??? ??, ??, ??
??? ??
Colorless liquid??
2,3-Dihydro-2,2-dimethyl-7-benzofuranol was used as starting reagent in the preparation of aminoalkanol derivatives of 2,3-dihydro-2,2-dimethyl-7-benzofuranol.?? ??
Odorless, white crystalline solid.?? ???
2,3-Dihydro-2,2-dimethyl-7-benzofuranol 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.2,3-Dihydro-2,2-dimethyl-7-benzofuranol ?? ?? ? ???
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O-?????
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2-?????
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2-[(2-??-2-????)??]-??
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?????(??)
1,2-Benzenediol, 4-(2-methyl-2-propen-1-yl)-
Phenol, 2-chloro-6-(2-methyl-1-propen-1-yl)-
?? ??
2,3-Dihydro-2,2-dimethyl-7-benzofuranol ?? ??
???( 206)?? ??
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