167592

Sigma-Aldrich

1-Chloro-2-methyl-2-propanol

97%

Synonym(s):
Chloro-tert-butyl alcohol
Linear Formula:
(CH3)2C(OH)CH2Cl
CAS Number:
Molecular Weight:
108.57
Beilstein/REAXYS Number:
1697054
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

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.

Packaging

50 mL in glass bottle

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Risk Statement

10

Safety Statement

23-24/25

RIDADR

UN 1987C 3 / PGIII

WGK Germany

WGK 3

Flash Point(F)

100.4 °F - closed cup

Flash Point(C)

38 °C - closed cup

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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