质量水平
检测方案
99%
形式
liquid
折射率
n20/D 1.524 (lit.)
bp
296-300 °C (lit.)
mp
23 °C (lit.)
密度
1.06 g/mL at 25 °C (lit.)
SMILES字符串
CCN(CC)C(=O)c1cccnc1
InChI
1S/C10H14N2O/c1-3-12(4-2)10(13)9-6-5-7-11-8-9/h5-8H,3-4H2,1-2H3
InChI key
NCYVXEGFNDZQCU-UHFFFAOYSA-N
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应用
N,N-二乙基烟酰胺(DENC)常用作制备四核铜配合物的配体。
警示用语:
Danger
危险声明
危险分类
Acute Tox. 3 Oral - Eye Irrit. 2
WGK
WGK 1
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Synthesis and properties of mixed-valence copper molecules (. mu.-Y) N4CuII2CUI2X4 (N= N, N-diethylnicotinamide; Y= 3, 4, 5, 6-tetrachlorocatecholate; X= Cl, Br, I) and the products and kinetics of their reactions with dioxygen and nitrobenzene.
Inorganic Chemistry, 29(24), 4891-4897 (1990)
Synthesis, structure and properties of the tetranuclear complexes [(DENC) CuX] 4 (DENC= N, N-diethylnicotinamide; X= Cl, Br, I) and the kinetics of oxidation of the chloride and bromide by dioxygen in aprotic solvents.
Inorganic Chemistry, 21(3), 995-1001 (1982)
Transmetalation reactions of tetranuclear copper (II) complexes. 2. Stoichiometry and products of reaction of [(DENC) CuCl] 4O2,[(DENC) CuCl] 4 (CO3) 2,[(DENC) CuCl] 4Cl4, and (DENC) 4Cu4Cl6O (DENC= N, N-diethylnicotinamide) with Ni (NS) 2, the kinetics of product isomerization in aprotic solvents, and inhibition of copper-catalyzed phenolic. oxidativecoupling by dioxygen through transmetalation.
Journal of the American Chemical Society, 106(16), 4596-4605 (1984)
Journal of controlled release : official journal of the Controlled Release Society, 93(2), 121-127 (2003-11-26)
New methods and pharmaceutical compositions were developed to increase the aqueous solubility of paclitaxel (PTX), a poorly water-soluble drug. Graft and star-shaped graft polymers consisting of poly(ethylene glycol) (PEG400) graft chains increased the PTX solubility in water by three orders
International journal of pharmaceutics, 314(2), 127-136 (2006-02-24)
The aim of this study was to prepare different types of paclitaxel-loaded, PLGA-based microparticles and lipidic implants, which can directly be injected into the brain tissue. Releasing the drug in a time-controlled manner over several weeks, these systems are intended
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