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170275

Sigma-Aldrich

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:
100-86-7
Molecular Weight:
150.22
Beilstein/REAXYS Number:
1855608
EC Number:
202-896-0
MDL number:
MFCD00004465
UNSPSC Code:
12352100
PubChem Substance ID:
24850290
NACRES:
NA.22

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.)

SMILES string

CC(C)(O)Cc1ccccc1

InChI

1S/C10H14O/c1-10(2,11)8-9-6-4-3-5-7-9/h3-7,11H,8H2,1-2H3

InChI key

RIWRBSMFKVOJMN-UHFFFAOYSA-N

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Application

2-Methyl-1-phenyl-2-propanol was used in the preparation of 2-methyl-1-phenyl-2-propyl bromide.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

177.8 °F - closed cup

flash_point_c

81 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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