推薦產品
化驗
98%
折射率
n20/D 1.422 (lit.)
bp
114-121 °C (lit.)
密度
0.746 g/mL at 25 °C (lit.)
SMILES 字串
C=CCCCCC=C
InChI
1S/C8H14/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-8H2
InChI 密鑰
XWJBRBSPAODJER-UHFFFAOYSA-N
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一般說明
1,7-辛二烯可作为乙烯的交联剂和来源,用于不同的Mori条件下的CEYM相关反应。
應用
用1,7-辛二烯研究了一系列简单的二前缀开环复分解的结构和反应速率。它也被用作研究等离子体聚合制备的微图案化表面。
訊號詞
Danger
危險聲明
危險分類
Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
50.0 °F - closed cup
閃點(°C)
10 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Langmuir : the ACS journal of surfaces and colloids, 33(35), 8790-8798 (2017-05-30)
The role surface capping molecules play in dictating the optical properties of semiconductor nanocrystals (NCs) is becoming increasingly evident. In this paper the role of surface capping molecule polarity on the optical properties of germanium NCs (Ge NCs) is explored.
ACS applied materials & interfaces, 11(31), 27615-27623 (2019-07-17)
The nature of the protein corona forming on biomaterial surfaces can affect the performance of implanted devices. This study investigated the role of surface chemistry and wettability on human serum-derived protein corona formation on biomaterial surfaces and the subsequent effects
Nanoscale, 8(8), 4635-4642 (2016-02-09)
The wetting of a material can be tuned by changing the roughness on its surface. Recent advances in the field of nanotechnology open exciting opportunities to control macroscopic wetting behaviour. Yet, the benchmark theories used to describe the wettability of
Nanoscale, 10(39), 18706-18719 (2018-10-03)
This study reports the preparation of functional bioinorganic hybrids, through application of the thiol-ene reaction, that exhibit catalytic activity and photoluminescent properties from enzymes and freestanding silicon nanocrystals. Thermal hydrosilylation of 1,7-octadiene and alkene-terminated poly(ethylene oxide)methyl ether with hydride-terminated silicon
Chemical communications (Cambridge, England), 46(38), 7145-7147 (2010-09-08)
In the RCM reactions of a series of simple α,ω-dienes, the relative order of reactivity has been unambiguously determined showing that cyclohexene forms faster than cyclopentene or cycloheptene. 1,5-Hexadiene inhibits the RCM of 1,7-octadiene; 1,5-hexadiene cannot progress to the RCM
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