B65586
2-溴乙醇
95%
别名:
乙烯溴醇
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关于此项目
线性分子式:
BrCH2CH2OH
化学文摘社编号:
分子量:
124.96
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-748-1
Beilstein/REAXYS Number:
878140
MDL number:
产品名称
2-溴乙醇, 95%
InChI key
LDLCZOVUSADOIV-UHFFFAOYSA-N
InChI
1S/C2H5BrO/c3-1-2-4/h4H,1-2H2
SMILES string
OCCBr
vapor density
4.3 (vs air)
vapor pressure
2.4 mmHg ( 20 °C)
assay
95%
form
liquid
refractive index
n20/D 1.492 (lit.)
bp
56-57 °C/20 mmHg (lit.)
density
1.763 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
2-溴乙醇可用于由乙酰化糖制备 2-溴乙基糖苷。它也可以用作合成 2-溴乙基甲氧基甲基醚的原料。
2-溴乙醇用于选择性还原硝基芳烃（PcFe（II）/NaBH4/2-溴乙醇催化剂体系）。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic 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
法规信息
危险化学品
此项目有
2-Bromoethyl glycosides: synthesis and characterisation.
Dahmen J, et al.
Carbohydrate Research, 116(2), 303-307 (1983)
Regio?and Stereoselective Intramolecular Hydrosilylation of α?Hydroxy Enol Ethers: 2, 3?syn?2?Methoxymethoxy?1, 3?Nonanediol: 1, 3?Nonanediol, 2?(methoxymethoxy)?,(R, R)?(?)?.
Tamao K, et al.
Organic Syntheses, 73, 94-94 (2003)
Ikuo Ueta et al.
Journal of chromatography. A, 1216(14), 2848-2853 (2008-11-18)
Fiber-packed sample preparation device was applied to the simultaneous derivatization/preconcentration of ethylene oxide (EO) in air samples. The polymer-coated filaments were packed longitudinally into the needle, and hydrogen bromide (HBr) was loaded onto the filaments in the preconditioning process. Simultaneous
H K Bhat et al.
Chemical research in toxicology, 3(4), 311-317 (1990-07-01)
The formation of fatty acid conjugates of haloethanols was studied under in vitro conditions by using purified bovine pancreatic cholesterol ester hydrolase (EC 3.1.1.13). The enzymatic formation of 2-chloroethyl and 2-bromoethyl esters of oleic, linoleic, linolenic, and arachidonic acids was
B J Ratliff et al.
The journal of physical chemistry. A, 114(14), 4934-4945 (2010-03-23)
This study photolytically generates, from 2-bromoethanol photodissociation, the 2-hydroxyethyl radical intermediate of the OH + ethene reaction and measures the velocity distribution of the stable radicals. We introduce an impulsive model to characterize the partitioning of internal energy in the
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