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Sigma-Aldrich

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:
3586-14-9
Molecular Weight:
184.23
Beilstein:
2045714
EC Number:
222-716-4
MDL number:
MFCD00008531
UNSPSC Code:
12352100
PubChem Substance ID:
57652711
NACRES:
NA.22

Assay

≥98.0% (GC)

form

liquid

refractive index

n20/D 1.573 (lit.)
n20/D 1.573

bp

271-273 °C (lit.)

density

1.051 g/mL at 25 °C (lit.)

SMILES string

Cc1cccc(Oc2ccccc2)c1

InChI

1S/C13H12O/c1-11-6-5-9-13(10-11)14-12-7-3-2-4-8-12/h2-10H,1H3

InChI key

UDONPJKEOAWFGI-UHFFFAOYSA-N

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Pictograms

Environment
GHS09

Hazard Statements

H411

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Chronic 2

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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