125903
1,3-二溴丙烷
99%, liquid, ReagentPlus®
别名:
三亚甲基二溴
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关于此项目
线性分子式:
Br(CH2)3Br
化学文摘社编号:
分子量:
201.89
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
203-690-3
MDL number:
Beilstein/REAXYS Number:
635662
产品名称
1,3-二溴丙烷, ReagentPlus®, 99%
InChI key
VEFLKXRACNJHOV-UHFFFAOYSA-N
InChI
1S/C3H6Br2/c4-2-1-3-5/h1-3H2
SMILES string
BrCCCBr
vapor density
7 (vs air)
product line
ReagentPlus®
assay
99%
form
liquid
refractive index
n20/D 1.524 (lit.)
bp
167 °C (lit.)
mp
−34 °C (lit.)
density
1.989 g/mL at 25 °C (lit.)
Quality Level
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Application
1,3-二溴丙烷可用于制备手性孪生双阳离子离子液体 和 1,3-双（1-7′-氯-4-喹啉基-4-哌嗪基）丙烷。3
General description
1,3-二溴丙烷是一种二卤代丙烷。在碳电极表面的聚合物膜中，它分别被电生液相镍 (I) 手性和镍 (I) 手性催化还原生成环丙烷和丙烯。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Flam. Liq. 3 - Skin Irrit. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
129.2 °F - closed cup
flash_point_c
54 °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
Catalytic reduction of α,ω-dihaloalkanes with nickel (I) salen as a homogeneous-phase and polymer-bound mediator.
Dahm CE and Peters DG.
Journal of Electroanalytical Chemistry, 406(1), 119-129 (1996)
Synthesis of Chiral Geminal Dicationic Ionic Liquid from Amino Acids.
Yin A, et al.
Asian Journal of Chemistry, 25(12), 6721-6721 (2013)
A Witkowski et al.
The Journal of biological chemistry, 267(26), 18488-18492 (1992-09-15)
Thioesterase II is a 29-kDa monomer which, in certain specialized tissues, acts as a chain terminator in fatty acid synthesis by hydrolyzing medium-chain fatty acids from the fatty acid synthase. As with serine proteases, hydrolysis appears to involve acylation of
E E Badr et al.
Journal of oleo science, 59(12), 647-652 (2010-11-26)
A fatty hydrazide based cationic gemini surfactants, 1,3-bis (N'-acyl-N,N-dimethylhydrazinium) propane dibromide which possess hydrolyzable amido moieties in the lipophilic portions, were prepared by reacting 1,3-bromopropane with N,N-dimethyl fatty hydrazide. The surface properties were explained and discussed based on the effect
S P James et al.
Toxicology letters, 8(1-2), 7-15 (1981-04-01)
Oral administration of 1,3-dibromopropane (2 mmol/kg) to rats resulted in a marked decrease in the level of hepatic glutathione (GSH). Sulphur-containing [14C]-metabolites were excreted in the bile of rats dose with 1,3-bromo[14C]propane and were subjected to enterohepatic cycling. After an
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