InChI key
YZUPZGFPHUVJKC-UHFFFAOYSA-N
InChI
1S/C3H7BrO/c1-5-3-2-4/h2-3H2,1H3
SMILES string
COCCBr
form
liquid
refractive index
n20/D 1.447 (lit.)
bp
40-41 °C/66 mmHg (lit.)
solubility
water: soluble 14.4 g/L at 25 °C
density
1.479 g/mL at 25 °C (lit.)
functional group
bromo
ether
storage temp.
2-8°C
Quality Level
Application
2-溴乙基甲基醚被已用作合成1-溴-4-(2-甲氧基乙氧基)苯和1-溴-4-[(2-甲氧基乙氧基)甲基]苯的起始试剂。
General description
已经研究了在丙酮中的碘化钾与2-溴乙基甲基醚在15和25℃下发生交换反应的动力学。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
82.4 °F - closed cup
flash_point_c
28 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Alex R Neale et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 18(15), 2040-2057 (2017-05-19)
A series of hydrophobic room temperature ionic liquids (ILs) based on ethereal functionalised pyrrolidinium, piperidinium and azepanium cations bearing the bis[(trifluoromethyl)sulfonyl]imide, [TFSI]
Novel water-soluble organosilane compounds as a radical reducing agent in aqueous media.
Yamazaki O, et al.
Bulletin of the Chemical Society of Japan, 70, 2519-2523 (1997)
Forrest S Gittleson et al.
Physical chemistry chemical physics : PCCP, 21(31), 17176-17189 (2019-07-26)
Ionic liquids are a unique class of materials with several potential applications in electrochemical energy storage. When used in electrolytes, these highly coordinating solvents can influence device performance through their high viscosities and strong solvation behaviors. In this work, we
Ulderico Ulissi et al.
ChemSusChem, 11(1), 229-236 (2017-09-30)
The room-temperature molten salt mixture of N,N-diethyl-N-(2-methoxyethyl)-N-methylammonium bis(trifluoromethanesulfonyl) imide ([DEME][TFSI]) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt is herein reported as electrolyte for application in Li-O
The Iodide Ion Exchange Reaction with 2-Haloethyl Alkyl Ethers and n-Butyl Bromide1.
Tutwiler FB and McKee RL.
Journal of the American Chemical Society, 76(24), 6342-6344 (1954)
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