All Photos(1)
Synonym(s):
2-(3-Methoxyphenyl)ethanol
Linear Formula:
CH3OC6H4CH2CH2OH
CAS Number:
Molecular Weight:
152.19
Beilstein:
1863114
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
refractive index
n20/D 1.538 (lit.)
bp
141-143 °C/12 mmHg (lit.)
density
1.075 g/mL at 25 °C (lit.)
SMILES string
COc1cccc(CCO)c1
InChI
1S/C9H12O2/c1-11-9-4-2-3-8(7-9)5-6-10/h2-4,7,10H,5-6H2,1H3
InChI key
UPPGEJSCUZMCMW-UHFFFAOYSA-N
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Related Categories
Application
3-Methoxyphenethyl alcohol was used as starting reagent during the synthesis of 3-methoxy-2,6-dimethyl- phenethyl alcohol.
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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An interesting synthesis of 3-methoxy-2, 6-dimethylphenethyl alcohol.
Meyer AL and Turner RB.
Tetrahedron, 27(13), 2609-2615 (1971)
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International journal of molecular sciences, 14(12), 23420-23440 (2013-11-30)
Melanin is responsible for skin color and plays a major role in defending against harmful external factors such as ultraviolet (UV) irradiation. Tyrosinase is responsible for the critical steps of melanogenesis, including the rate-limiting step of tyrosine hydroxylation. The mechanisms
Min Kyung Song et al.
Journal of agricultural and food chemistry, 67(7), 2028-2035 (2019-01-31)
Caffeic acid phenethyl ester (CAPE) is an ester of a hydroxycinnamic acid (phenylpropanoid) and a phenylethanoid (2-phenylethanol; 2-PE), which has long been used in traditional medicine. Here, we synthesized 54 hydroxycinnamic acid-phenylethanoid esters by feeding 64 combinations of hydroxycinnamic acids
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