167592
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:
Molecular Weight:
108.57
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-196-4
Beilstein/REAXYS Number:
1697054
MDL number:
Assay:
97%
InChI key
JNOZGFXJZQXOSU-UHFFFAOYSA-N
InChI
1S/C4H9ClO/c1-4(2,6)3-5/h6H,3H2,1-2H3
SMILES string
CC(C)(O)CCl
assay
97%
Quality Level
bp
124-128 °C (lit.)
density
1.058 g/mL at 25 °C (lit.)
functional group
chloro, hydroxyl
Related Categories
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.
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
100.4 °F - closed cup
flash_point_c
38 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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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