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质量水平
方案
99%
表单
liquid
折射率
n20/D 1.446 (lit.)
沸点
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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Danger
危险声明
危险分类
Flam. Liq. 3 - Skin Corr. 1B
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
123.8 °F - closed cup
闪点(°C)
51 °C - closed cup
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
Daria Kupczyk et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-19)
Glucocorticoid metabolism at the tissue level is regulated by two isoenzymes 11β-hydroxysteroid dehydrogenase (11β-HSD), which mutually convert biologically active cortisol and inactive cortisone. Recent research is focused on the role of 11β-HSD1 and 11β-HSD2 as autocrine factors of tumor cell
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