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167592

Sigma-Aldrich

1-Chloro-2-methyl-2-propanol

97%

Synonym(s):

Chloro-tert-butyl alcohol

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About This Item

Linear Formula:
(CH3)2C(OH)CH2Cl
CAS Number:
558-42-9
Molecular Weight:
108.57
Beilstein/REAXYS Number:
1697054
EC Number:
209-196-4
MDL number:
MFCD00021807
UNSPSC Code:
12352100
PubChem Substance ID:
24850217
NACRES:
NA.22

Quality Level

100

assay

97%

refractive index

n20/D 1.439 (lit.)

bp

124-128 °C (lit.)

density

1.058 g/mL at 25 °C (lit.)

SMILES string

CC(C)(O)CCl

InChI

1S/C4H9ClO/c1-4(2,6)3-5/h6H,3H2,1-2H3

InChI key

JNOZGFXJZQXOSU-UHFFFAOYSA-N

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General description

Reaction of 1-chloro-2-methyl-2-propanol on oxygen-containing Ag(110) surfaces has been investigated by synchrotron-based temperature-programmed X-ray photoelectron spectroscopy.

Application

1-Chloro-2-methyl-2-propanol was used in the synthesis and characterization of new polyfunctional thiols.

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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2-Chloro-2-methylpropane 99%

Sigma-Aldrich

C56352

2-Chloro-2-methylpropane

2-Methyl-1-propanol anhydrous, 99.5%

Sigma-Aldrich

294829

2-Methyl-1-propanol

Dimethyl carbonate anhydrous, ≥99%

Sigma-Aldrich

517127

Dimethyl carbonate

tert-Butanol anhydrous, ≥99.5%

Sigma-Aldrich

471712

tert-Butanol

Multistep reaction processes in epoxide formation from 1-chloro-2-methyl-2-propanol on Ag (110) revealed by TPXPS and TPD experiments.
Piao H, et al.
The Journal of Physical Chemistry B, 107(50), 13976-13985 (2003)
Catherine Vermeulen et al.
Combinatorial chemistry & high throughput screening, 9(8), 583-590 (2006-10-05)
Combinatorial chemistry was shown to be an efficient tool for the preparation of new aroma-impact compounds. In this case, polyfunctional thiols were synthesized quickly using halide reagents or Bunte salt intermediates. They were separated by gas chromatography and then characterized

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