77780
3-Phenoxytoluene
≥98.0% (GC)
Synonym(s):
3-Methyldiphenyl ether, Phenyl m-tolyl ether
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About This Item
Linear Formula:
C6H5OC6H4CH3
CAS Number:
Molecular Weight:
184.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
222-716-4
Beilstein/REAXYS Number:
2045714
MDL number:
Assay:
≥98.0% (GC)
Form:
liquid
InChI key
UDONPJKEOAWFGI-UHFFFAOYSA-N
InChI
1S/C13H12O/c1-11-6-5-9-13(10-11)14-12-7-3-2-4-8-12/h2-10H,1H3
SMILES string
Cc1cccc(Oc2ccccc2)c1
assay
≥98.0% (GC)
form
liquid
bp
271-273 °C (lit.)
density
1.051 g/mL at 25 °C (lit.)
functional group
phenoxy
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 2
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
266.0 °F - Pensky-Martens closed cup
flash_point_c
130 °C - Pensky-Martens closed cup
ppe
Eyeshields, Gloves
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S Schmidt et al.
FEMS microbiology letters, 75(2-3), 253-258 (1992-09-15)
The bacterium Sphingomonas sp. SS31, which was obtained from the diphenyl ether-degrading strain Sphingomonas sp. SS3 by an adaptation process, utilized 3-methyldiphenyl ether for growth in addition to diphenyl ether. The initial enzymatic attack onto this compound proceeded by a
Liqing Zhao et al.
Applied microbiology and biotechnology, 91(4), 989-999 (2011-05-13)
Cytochrome P450s are synthetically attractive hydroxylation catalysts. For cell-free applications, a constant supply of NAD(P)H can be very costly. Mediators such as Zn/Co(III)sep can be an alternative cofactor system to NAD(P)H. Several mutants of cytochrome P450 BM3 with improved electron
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