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Thermo Scientific Chemicals
Veratrole, 99%
CAS: 91-16-7 | C8H10O2 | 138.166 g/mol
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化學識別
CAS91-16-7
IUPAC Name1,2-dimethoxybenzene
Molecular FormulaC8H10O2
InChI KeyABDKAPXRBAPSQN-UHFFFAOYSA-N
SMILESCOC1=CC=CC=C1OC
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規格
規格表
規格表FormLiquid as melt
Assay (GC)≥98.5%
Identification (FTIR)Conforms
Refractive Index1.5320-1.5350 @ 20?C
Appearance (Color)Clear colorless to pale yellow
It is useful for organic synthesis of aromatic compounds. Veratrole is relatively electron-rich and thus readily undergoes electrophilic substitution.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
It is useful for organic synthesis of aromatic compounds. Veratrole is relatively electron-rich and thus readily undergoes electrophilic substitution.
Solubility
Soluble in alcohol, diethyl ether, acetone, and methanol. Slightly soluble in water.
Notes
Store at room temperature. Keep away from oxidizing agents.
It is useful for organic synthesis of aromatic compounds. Veratrole is relatively electron-rich and thus readily undergoes electrophilic substitution.
Solubility
Soluble in alcohol, diethyl ether, acetone, and methanol. Slightly soluble in water.
Notes
Store at room temperature. Keep away from oxidizing agents.
RUO – Research Use Only
General References:
- Biju M. Devassy.; S.B. Halligudi. Zirconia-supported heteropoly acids: Characterization and catalytic behavior in liquid-phase veratrole benzoylation.J. Catal. 2005, 236 (2),313-323.
- Irene M. Matheson (née Davidson).;O. C. Musgrave.; C. J. Webster. Oxidation of veratrole by quinones. Chem. Commun. (London). 1965, (13), 278-279.
- In contrast to 1,3-Dimethoxybenzene, A13380, direct dilithiation with n-BuLi + TMEDA is feasible, giving, after reaction with TMS chloride, the 3,6-disilyl derivative as the major product in 50-60% yield: J. Org. Chem., 49, 4657 (1984).