270768
4-叔丁基苄溴
97%
别名:
α-溴-4-叔丁基甲苯, 1-溴甲基-4-叔丁基苯
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关于此项目
线性分子式:
(CH3)3CC6H4CH2Br
化学文摘社编号:
分子量:
227.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
242-643-1
Beilstein/REAXYS Number:
471674
MDL number:
产品名称
4-叔丁基苄溴, 97%
InChI key
QZNQSIHCDAGZIA-UHFFFAOYSA-N
InChI
1S/C11H15Br/c1-11(2,3)10-6-4-9(8-12)5-7-10/h4-7H,8H2,1-3H3
SMILES string
CC(C)(C)c1ccc(CBr)cc1
assay
97%
form
liquid
refractive index
n20/D 1.545 (lit.)
bp
93-94 °C/1.5 mmHg (lit.)
mp
8-12 °C (lit.)
density
1.236 g/mL at 25 °C (lit.)
functional group
bromo
Quality Level
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Application
4-叔丁基苄基溴是一种疏水性反应物，用于在连续搅拌下保持负载介孔材料颗粒。
General description
4-叔丁基苄基溴和碘化钾的亲核取代反应是在基于各种表面活性剂的水包油微乳中进行的。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Tomasz Witula et al.
Journal of colloid and interface science, 310(2), 536-545 (2007-03-03)
Mesoporous materials have been investigated as auxiliary agents for organic synthesis comprising reactants with widely different solubility characteristics. The finely divided oxide material was immersed in an aqueous solution of a water-soluble reactant, potassium iodide, and the loaded particles were
Maria Häger et al.
Langmuir : the ACS journal of surfaces and colloids, 20(15), 6107-6115 (2004-07-14)
A nucleophilic substitution reaction between 4-tert-butylbenzyl bromide and potassium iodide has been performed in oil-in-water microemulsions based on various C12Em surfactants, i.e., dodecyl ethoxylate with m number of oxyethylene units. The reaction kinetics was compared with the kinetics of reactions
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