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About This Item
Linear Formula:
(CH3)2C6H3OCH3
CAS Number:
Molecular Weight:
136.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
99%
form
liquid
refractive index
n20/D 1.517 (lit.)
bp
200-201 °C (lit.)
density
0.974 g/mL at 25 °C (lit.)
SMILES string
COc1ccc(C)c(C)c1
InChI
1S/C9H12O/c1-7-4-5-9(10-3)6-8(7)2/h4-6H,1-3H3
InChI key
LVUBSVWMOWKPDJ-UHFFFAOYSA-N
Application
3,4-Dimethylanisole was used as starting reagent in the synthesis of 3- and 4-methoxy-N-hydroxyphthalimide.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
168.8 °F - closed cup
Flash Point(C)
76 °C - closed cup
Certificates of Analysis (COA)
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N-Hydroxyphthalimide/Cobalt (II) Catalyzed Low Temperature Benzylic Oxidation Using Molecular Oxygen.
Wentzel BB, et al.
Tetrahedron, 56(39), 7797-7803 (2000)
Kamila K Mentel et al.
Nature communications, 9(1), 2903-2903 (2018-07-27)
Electron transfer reactions are arguably the simplest chemical reactions but they have not yet ceased to intrigue chemists. Charge-separation and charge-recombination reactions are at the core of life-sustaining processes, molecular electronics and solar cells. Intramolecular electron donor-acceptor systems capture the
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