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
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)
2-Bromoethyl glycosides: synthesis and characterisation.
Dahmen J, et al.
Carbohydrate Research, 116(2), 303-307 (1983)
H Dunkelberg
Zentralblatt fur Bakteriologie, Mikrobiologie und Hygiene. 1. Abt. Originale B, Hygiene, 177(3-4), 269-281 (1983-04-01)
The compounds 2-chloroethanol and 2-bromoethanol were administered once weekly subcutaneously to groups of 100 female NMRI mice, in the case of 2-chloroethanol in 3 dosages (3.0, 1.0 and 0.3 mg, single dosage per mouse) and 2-bromoethanol in 2 dosages (1.0
Caroline C Womack et al.
The journal of physical chemistry. A, 115(51), 14559-14569 (2011-11-11)
This work characterizes the internal energy distribution of the CD(2)CD(2)OH radical formed via photodissociation of 2-bromoethanol-d(4). The CD(2)CD(2)OH radical is the first radical adduct in the addition of the hydroxyl radical to C(2)D(4) and the product branching of the OH
S Khan et al.
Pharmacology & toxicology, 78(4), 241-248 (1996-04-01)
The cytotoxicity of 2-bromoethanol towards hepatocytes isolated from rats was concentration-dependent (EC(50)100 mu M, 2 hr). Bromoacetaldehyde was more toxic (EC(50)60 mu M, 2 hr) and bromoacetic acid was less toxic (EC(50)150 mu M, 2 hr). Glutathione (GSH) depletion occurred
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