方案
≥98.0% (GC)
表单
liquid
折射率
n20/D 1.570
沸点
177 °C/8 mmHg (lit.)
mp
24 °C (lit.)
官能团
ester
phenyl
SMILES字符串
O=C(OCc1ccccc1)c2cccnc2
InChI
1S/C13H11NO2/c15-13(12-7-4-8-14-9-12)16-10-11-5-2-1-3-6-11/h1-9H,10H2
InChI key
KVYGGMBOZFWZBQ-UHFFFAOYSA-N
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一般描述
Benzyl nicotinate is a benzyl ester. It is a vasodilator agent and is also generally used in cosmetics and drugs.
应用
Benzyl nicotinate can be used for the synthesis of benzylpalladium complexes to be used as catalysts for the substitution of olefins with benzylic groups.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Julijana Kristl et al.
AAPS pharmSci, 5(1), E2-E2 (2003-04-26)
New and improved drug delivery systems are the important subject of much scientific research. The development of formulations that increase skin oxygenation and of methods for measuring oxygen levels in skin are important for dealing with healing processes affected by
Zrinka Abramovic et al.
Advances in experimental medicine and biology, 701, 75-82 (2011-03-30)
Tumor hypoxia is a well known therapeutic problem which contributes to radioresistance and aggressive tumor characteristics. Lack of techniques for repeated measurements of tumor oxygenation (pO(2), partial pressure of oxygen) has restricted the optimization of hypoxia modifying methods and their
Synthesis of benzylpalladium complexes through C-O bond cleavage of benzylic carboxylates: Development of a novel palladium-catalyzed benzylation of olefins.
Narahashi H, et al.
Journal of Organometallic Chemistry, 693(2), 283-296 (2008)
V Erjavec et al.
International journal of pharmaceutics, 307(1), 1-8 (2005-11-01)
The purpose of this study was to select the best types of liposomes for use as drug carriers for topical treatment of oral mucosal lesions. Electron paramagnetic resonance (EPR) oximetry, using the paramagnetic probe lithium phthalocyanine, was used in vivo
Efficient transesterification/acylation reactions mediated by N-heterocyclic carbene catalysts.
Grasa GA, et al.
The Journal of Organic Chemistry, 68(7), 2812-2819 (2003)
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