2,3-Dihydro-2,2-dimethyl-7-benzofuranol

2,3-Dihydro-2,2-dimethyl-7-benzofuranol Basic information

Product Name:	2,3-Dihydro-2,2-dimethyl-7-benzofuranol
Synonyms:	2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-ol;2,3-DIHYDRO-2,2-DIMETHYL-7-HYDROXYBENZOFURAN;2,3-DIHYDRO-2,2-DIMETHYLBENZOFURAN-7-OL;2,3-DIHYDRO-2,2-DIMETHYL-7-BENZOFURANOL;2,2-DIMETHYL-7-HYDROXYCOUMARAN;2,2-DIMETHYL-2,3-DIHYDRO-BENZOFURAN-7-OL;2,3-DIHYDRO-2,2-DIMETHYLBENZOFURAN-7-OL, 1GM, NEAT;CARBOFURANPHENOL(2,3-DIHYDRO-2,2-DIMETHYL-7-HYDROXYBENZOFURANOL)
CAS:	1563-38-8
MF:	C10H12O2
MW:	164.2
EINECS:	216-350-4
Product Categories:	Miscellaneous;Furan&Benzofuran;Alphabetic;D;DID - DINEnvironmental Standards;Metabolites;Benzofurans;Building Blocks;Heterocyclic Building Blocks;Pesticides&Metabolites
Mol File:	1563-38-8.mol

2,3-Dihydro-2,2-dimethyl-7-benzofuranol Chemical Properties

Boiling point	95°C 1mm
density	1.101 g/mL at 25 °C (lit.)
refractive index	n20/D 1.541(lit.)
Fp	>230 °F
storage temp.	2-8°C
solubility	Chloroform (Slightly), Methanol (Sparingly)
pka	10.10±0.40(Predicted)
form	Oil
color	Colourless
Specific Gravity	1.101
CAS DataBase Reference	1563-38-8(CAS DataBase Reference)
NIST Chemistry Reference	7-Benzofuranol, 2,3-dihydro-2,2-dimethyl-(1563-38-8)
EPA Substance Registry System	2,3-Dihydro-2,2-dimethyl-7-benzofuranol (1563-38-8)

Safety Information

MSDS Information

Provider	Language
Dihydro-2,2-dimethyl-7-benzofuranol	English
SigmaAldrich	English

2,3-Dihydro-2,2-dimethyl-7-benzofuranol Usage And Synthesis

Chemical Properties	Colorless liquid
Uses	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.
Definition	ChEBI: 2,2-dimethyl-2,3-dihydro-1-benzofuran-7-ol is a member of 1-benzofurans.
General Description	Odorless, white crystalline solid.
Reactivity Profile	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 Preparation Products And Raw materials

Raw materials	Hydrochloric acid-->Sodium carbonate-->Phenol-->Oleic acid-->Cyclohexanone-->Acetophenone-->Isobutylene-->Catechol-->Carbofuran-->Guaiacol-->Benzofuran-->2-Nitrophenol-->2-Chlorophenol-->3-Chloro-2-methylpropene-->2-Isopropylphenol-->2-[(2-METHYL-2-PROPENYL)OXY]-PHENOL-->1,2-Benzenediol, 4-(2-methyl-2-propen-1-yl)--->Phenol, 2-chloro-6-(2-methyl-1-propen-1-yl)-
Preparation Products	Carbofuran

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