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About This Item
Linear Formula:
C6H5CH(OCH3)CH2OH
CAS Number:
Molecular Weight:
152.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
99%
form
liquid
refractive index
n20/D 1.519 (lit.)
bp
237 °C (lit.)
density
1.061 g/mL at 25 °C (lit.)
functional group
ether
hydroxyl
phenyl
SMILES string
COC(CO)c1ccccc1
InChI
1S/C9H12O2/c1-11-9(7-10)8-5-3-2-4-6-8/h2-6,9-10H,7H2,1H3
InChI key
JDTUPLBMGDDPJS-UHFFFAOYSA-N
Application
(S)-2-methoxy-2-phenylethanol was employed as chiral probe for the determination of absolute configuration of active (-) enantiomer of amlodipine. 2-Methoxy-2-phenylethanol was also used in the synthesis of optically active 1,4-dihydropyridines.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
208.4 °F - closed cup
Flash Point(C)
98 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Enzymatic resolution of the chiral inductor 2-methoxy-2-phenylethanol.
Monterde MI, et al.
Tetrahedron Asymmetry, 13(10), 1091-1096 (2002)
S Goldmann et al.
Journal of medicinal chemistry, 35(18), 3341-3344 (1992-09-04)
The active (-) enantiomer of amlodipine was originally reported to have R configuration. This does not concur with other 1,4-dihydropyridines with known absolute configuration. This configuration has now been determined by X-ray structural analysis using (1S)-camphanic acid and (S)-2-methoxy-2-phenylethanol as
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