170275
2-Methyl-1-phenyl-2-propanol
98%
Synonym(s):
1,1-Dimethyl-2-phenylethyl alcohol, Benzyl dimethyl carbinol
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About This Item
Linear Formula:
C6H5CH2C(CH3)2OH
CAS Number:
Molecular Weight:
150.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-896-0
Beilstein/REAXYS Number:
1855608
MDL number:
Product Name
2-Methyl-1-phenyl-2-propanol, 98%
InChI key
RIWRBSMFKVOJMN-UHFFFAOYSA-N
InChI
1S/C10H14O/c1-10(2,11)8-9-6-4-3-5-7-9/h3-7,11H,8H2,1-2H3
SMILES string
CC(C)(O)Cc1ccccc1
assay
98%
form
solid
refractive index
n20/D 1.514 (lit.)
bp
94-96 °C/10 mmHg (lit.)
mp
23-25 °C (lit.)
density
0.974 g/mL at 25 °C (lit.)
Quality Level
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Application
2-Methyl-1-phenyl-2-propanol was used in the preparation of 2-methyl-1-phenyl-2-propyl bromide.
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David C Magri et al.
Organic & biomolecular chemistry, 1(19), 3418-3429 (2003-10-31)
Two dialkyl peroxides, devised as kinetic probes for the heterogeneous electron transfer (ET), are studied using heterogeneous and homogeneous electrochemical techniques. The peroxides react by concerted dissociative ET reduction of the O-O bond. Under heterogeneous conditions, the only products isolated
Takao Raku et al.
Biotechnology letters, 26(8), 665-670 (2004-06-18)
For the purpose of developing a new synthetic polymer containing an asymmetric molecule branch, three racemic alcohols, i.e. 1-phenylethanol, 1-(4-methylphenyl)ethanol and 1-(2-naphthyl)ethanol, were esterified enzymatically with divinyladipate using a lipase from Pseudomonas cepacia. The enzymatic acylation of alcohols produced monoacylated
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