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167592

Sigma-Aldrich

1-Chloro-2-methyl-2-propanol

97%

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Synonym(s):
Chloro-tert-butyl alcohol
Linear Formula:
(CH3)2C(OH)CH2Cl
CAS Number:
558-42-9
Molecular Weight:
108.57
Beilstein:
1697054
EC Number:
209-196-4
MDL number:
MFCD00021807
PubChem Substance ID:
24850217
NACRES:
NA.22

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

Signal Word

Warning

Hazard Statements

H226

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

100.4 °F - closed cup

Flash Point(C)

38 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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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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