187933
3-Methoxyphenethyl alcohol
97%
Synonym(s):
2-(3-Methoxyphenyl)ethanol
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
CH3OC6H4CH2CH2OH
CAS Number:
Molecular Weight:
152.19
Beilstein/REAXYS Number:
1863114
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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.)
functional group
hydroxyl
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
3-Methoxyphenethyl alcohol was used as starting reagent during the synthesis of 3-methoxy-2,6-dimethyl- phenethyl alcohol.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
An interesting synthesis of 3-methoxy-2, 6-dimethylphenethyl alcohol.
Meyer AL and Turner RB.
Tetrahedron, 27(13), 2609-2615 (1971)
Kuo-Ching Wen et al.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service