189316
3-Chloro-2,2-dimethyl-1-propanol
99%
Sinónimos:
2-Chloromethyl-2-methyl-1-propanol
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About This Item
Fórmula lineal:
ClCH2C(CH3)2CH2OH
Número de CAS:
Peso molecular:
122.59
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
99%
refractive index
n20/D 1.45 (lit.)
bp
87 °C/35 mmHg (lit.)
mp
34-36 °C (lit.)
functional group
chloro
hydroxyl
SMILES string
CC(C)(CO)CCl
InChI
1S/C5H11ClO/c1-5(2,3-6)4-7/h7H,3-4H2,1-2H3
InChI key
CAZPRAORHCOIHC-UHFFFAOYSA-N
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General description
3-Chloro-2,2-dimethyl-1-propanol undergoes oxidation with pyridinium chlorochromate to yield 3-chloro-2,2-dimethylpropanal which spontaneously trimerizes to s-trioxane.
Application
3-Chloro-2,2-dimethyl-1-propanol has been used in combinatorial preparation of new aroma-impact compounds such as polyfunctional thiols.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
159.8 °F - closed cup
flash_point_c
71 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
2, 4, 6-Tri (2'-chloro-1', 1'-dimethylethyl)-s-trioxane: Synthesis, Spectroscopy and Crystal Structure.
Tarbutton GL and Valente EJ.
Journal of Chemical Crystallography, 40(2), 126-129 (2010)
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
Xin Min et al.
Royal Society open science, 5(5), 180156-180156 (2018-06-13)
A novel alkyl lithium-based initiator with relatively large steric hindrance, tert-butyldimethylsiloxydimethylpropyl lithium (TBDMSODPrLi), was designed and synthesized. By using TBDMSODPrLi, hydroxyl-terminated polybutadiene (HTPB) was prepared via anionic polymerization. The macromolecular structure of HTPB was characterized and verified by FTIR and
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