所有图片(2)
About This Item
经验公式(希尔记法):
C8H14N2O2
CAS号:
分子量:
170.21
Beilstein:
908482
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
≥97.0%
表单
liquid
折射率
n20/D 1.464
密度
1.041 g/mL at 20 °C (lit.)
官能团
ether
储存温度
2-8°C
SMILES字符串
CCOC(OCC)n1ccnc1
InChI
1S/C8H14N2O2/c1-3-11-8(12-4-2)10-6-5-9-7-10/h5-8H,3-4H2,1-2H3
InChI key
NNQBAGFIYBBAFL-UHFFFAOYSA-N
一般描述
原酰胺保护的咪唑。二价阴离子选择性地在 2 位反应
应用
1-(Diethoxymethyl)imidazole may be used in the preparation of various hydroxy- and amino-functionalized imidazoles, via isoprene-mediated lithiation followed by reaction with an electrophile.
警示用语:
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
233.6 °F
闪点(°C)
112.0 °C
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
1, 2-Functionalized Imidazoles as Palladium Ligands: An Efficient and Robust Catalytic System for the Fluorine-Free Hiyama Reaction.
Martinez R, et al.
European Journal of Organic Chemistry, 4, 872-877 (2014)
N.J. Curtis et al.
The Journal of Organic Chemistry, 45, 4038-4038 (1980)
Isoprene-catalysed lithiation: deprotection and functionalisation of imidazole derivatives.
Torregrosa R, et al.
Tetrahedron, 63(4), 947-952 (2007)
L.N. Pridgen et al.
Tetrahedron Letters, 38, 1275-1275 (1997)
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