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线性分子式:
BrC6H4CH2CH2OH
化学文摘社编号:
分子量:
201.06
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
liquid
InChI
1S/C8H9BrO/c9-8-3-1-2-7(6-8)4-5-10/h1-3,6,10H,4-5H2
SMILES string
OCCc1cccc(Br)c1
InChI key
PTTFLKHCSZSFOL-UHFFFAOYSA-N
assay
99%
form
liquid
refractive index
n20/D 1.5732 (lit.)
bp
107-110 °C/1 mmHg (lit.)
density
1.478 g/mL at 25 °C (lit.)
functional group
bromo, hydroxyl
Quality Level
General description
3-Bromophenethyl alcohol is a phenethyl alcohol derivative. Its enthalpy of vaporization at boiling point has been determined.
Application
3-Bromophenethyl alcohol may be used as a starting material in the synthesis of its mesylate derivative (m-Br-C6H4CH2CH2OMs) by treatment with mesyl chloride.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Annie Tam et al.
Bioorganic & medicinal chemistry, 17(3), 1055-1063 (2008-03-04)
The traceless Staudinger ligation can be mediated by phosphinothiols under physiological conditions. Proximal positive charges are necessary to achieve that transformation, presumably because those charges discourage protonation of the key iminophosphorane intermediate. Here, a series of cationic phosphinothiols is used
Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 466-466 (2008)
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