推荐产品
质量水平
检测方案
99%
形式
liquid
折射率
n20/D 1.446 (lit.)
bp
156-160 °C (lit.)
密度
1.394 g/mL at 25 °C (lit.)
SMILES字符串
CCOC(=O)C(C)Br
InChI
1S/C5H9BrO2/c1-3-8-5(7)4(2)6/h4H,3H2,1-2H3
InChI key
ARFLASKVLJTEJD-UHFFFAOYSA-N
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警示用语：
Danger
危险声明
危险分类
Flam. Liq. 3 - Skin Corr. 1B
WGK
WGK 3
闪点(°F)
123.8 °F
闪点(°C)
51 °C
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
Shengtao Lu et al.
Nature communications, 9(1), 4277-4277 (2018-10-17)
An intelligent drug release system that is triggered into action upon sensing the motion of swarmer P. mirabilis is introduced. The rational design of the drug release system focuses on a pNIPAAm-co-pAEMA copolymer that prevents drug leakage in a tobramycin-loaded
Sai Chen et al.
Polymers, 11(7) (2019-07-04)
Shape-stabilized phase change materials (SPCMs) are green, reusable energy storage materials. Because the melting temperature of n-alkyl acrylate copolymer is adjustable by controlling the side-chain length, the appropriate melting temperature can be achieved. Poly(tetradecyl acrylate-co-hexadecyl acrylate) (P(TDA-co-HDA)) with a molar
Cansu Aydogan et al.
Macromolecular rapid communications, 40(14), e1900109-e1900109 (2019-05-16)
A straightforward transformation protocol combining two distinct living polymerization methods for the controlled synthesis of block copolymers is described. In the first step, bromo-terminated poly(methyl methacrylate) is prepared by atom transfer radical polymerization (ATRP). Then, a bromide end group is
Ceren Kütahya et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(46), 10444-10451 (2020-04-29)
NIR exposure at 790 nm activated photopolymerization of monomers comprising UV-absorbing moieties by using [CuII /(TPMA)]Br2 (TPMA=tris(2-pyridylmethyl)amine) in the ppm range and an alkyl bromide as initiator. Some of them comprised structural elements selected either from those showing proton transfer or
David J S Patinha et al.
Talanta, 198, 193-199 (2019-03-17)
In this work, a facile preparation of SPME fibers with increased surface area is presented. The SPME fibers were prepared by grinding poly(ionic liquids) (PILs) to obtain particles of 1-16 µm and, with the aid of a silicon adhesive, attach these
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