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50 ML
$110.60
About This Item
Linear Formula:
C2H5CH(CH3)CH2Cl
CAS Number:
Molecular Weight:
106.59
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
$110.60
List Price$158.00Save 30%Web-Only Promotion
Available to ship onApril 15, 2025Details
Request a Bulk Order
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Quality Level
assay
96%
refractive index
n20/D 1.412 (lit.)
bp
100 °C/750 mmHg (lit.)
density
0.886 g/mL at 25 °C (lit.)
functional group
alkyl halide
chloro
SMILES string
CCC(C)CCl
InChI
1S/C5H11Cl/c1-3-5(2)4-6/h5H,3-4H2,1-2H3
InChI key
IWAKWOFEHSYKSI-UHFFFAOYSA-N
Related Categories
General description
1-Chloro-2-methylbutane is a halogenated organic building block. It can be synthesized by employing 2-methylbutanol as starting reagent.[1] Grignard reagent derived from (+)-1-chloro-2-methylbutane may be employed for the preparation of partially optically active (-)-alkylphenylcarbinols[2] and partially optically active secondary carbinols.[3] Infrared and Raman spectra of its optically active form (+)(S)-1-chloro-2-methylbutane in various phases (liquid, glass and crystal) have been evaluated.[4]
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Infrared and Raman spectra and normal frequencies calculation of isomeric (+)(S)-1-chloro-2-methylbutane.
Schettino V and Benedetti E.
Spectrochimica Acta Part A: Molecular Spectroscopy, 34(3), 353-356 (1978)
Asymmetric Reductions. VI. The Action of the Grignard Reagent from (+)-1-Chloro-2-methylbutane on a Series of Alkyl t-Butyl Ketones1.
Foley WM, et al.
Journal of the American Chemical Society, 81(11), 2779-2784 (1959)
Asymmetric Reductions. VII. the Action of the Grignard Reagent from (+)-1-chloro-2-methylbutane on a Series of Alkyl Phenyl Ketones1-3.
MacLeod R, et al.
Journal of the American Chemical Society, 82(4), 876-880 (1960)
Synthetic inhibitors of Alcohol dehydrogenase. 4-Substituted alkyl and cycloalkylpyrazoles.
Tolf BR, et al.
Acta Chemica Scandinavica, 33, 483-487 (1979)
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