所有图片(1)
About This Item
经验公式（希尔记法）:
C8H8O
CAS号:
分子量:
120.15
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
质量水平
方案
97%
表单
liquid
折射率
n20/D 1.522 (lit.)
密度
0.978 g/mL at 25 °C (lit.)
官能团
phenoxy
储存温度
2-8°C
SMILES字符串
C=COc1ccccc1
InChI
1S/C8H8O/c1-2-9-8-6-4-3-5-7-8/h2-7H,1H2
InChI key
NHOGGUYTANYCGQ-UHFFFAOYSA-N
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Sens. 1
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
60.8 °F
闪点(°C)
16 °C
法规信息
危险化学品
Hee-Kwon Kim et al.
ACS applied materials & interfaces, 5(12), 5648-5658 (2013-06-19)
Novel pH-responsive assemblies (PEG-lipid:DOPE liposomes) containing tunable and bifunctional phenyl-substituted vinyl ether (PIVE) cross-linkers were prepared. The assemblies consisted of 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), acid-cleavable poly(ethylene glycol) (PEG)-conjugated lipids, pDNA, and protamine sulfate (PS). The PIVE linkage was designed to hydrolyze under
Shihua Wang et al.
Organic letters, 13(22), 5968-5971 (2011-10-20)
Benzo[b]furans were prepared in one pot based on the addition/palladium-catalyzed C-H bond functionalization of phenols with bromoalkynes. The addition reactions of phenols to bromoalkynes generated (Z)-2-bromovinyl phenyl ethers in high yields with excellent regio- and stereoselectivity. The obtained (Z)-2-bromovinyl phenyl
M Isobe et al.
The Journal of toxicological sciences, 20(2), 161-164 (1995-05-01)
4-Nitrophenyl vinyl ether (NPVE) and phenyl vinyl ether (PVE) administered i.p. in mice lowered hepatic non-protein sulfhydryl (NP-SH) content, but did not elevate the serum glutamate pyruvate transaminase (GPT) activity. n-Butyl vinyl ether (BVE) showed no significant effects either on
Christopher L Rock et al.
Dalton transactions (Cambridge, England : 2003), 48(2), 461-467 (2018-11-30)
The phosphine-substituted α-diimine Ni precursor, (Ph2PPrDI)Ni, has been found to catalyze alkene hydrosilylation in the presence of Ph2SiH2 with turnover frequencies of up to 124 h-1 at 25 °C (990 h-1 at 60 °C). Moreover, the selective hydrosilylation of allylic
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