23021
2-(2-氯乙氧基)四氢-2H-吡喃
≥97.0%
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关于此项目
经验公式（希尔记法）:
C7H13ClO2
化学文摘社编号:
分子量:
164.63
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
1280441
MDL number:
SMILES string
ClCCOC1CCCCO1
InChI
1S/C7H13ClO2/c8-4-6-10-7-3-1-2-5-9-7/h7H,1-6H2
InChI key
ZVVQFPGYDBUGQB-UHFFFAOYSA-N
assay
≥97.0%
refractive index
n20/D 1.459
bp
80 °C/8 mmHg (lit.)
density
1.115 g/mL at 20 °C (lit.)
General description
用于引入 2-羟基乙基保护基团的结构单元
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
149.0 °F - closed cup
flash_point_c
65 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
B. Son et al.
Synthesis, 776-776 (1984)
H Ikuta et al.
Journal of medicinal chemistry, 30(11), 1995-1998 (1987-11-01)
A series of 3-(3,5-di-tert-butyl-4-hydroxybenzylidene)pyrrolidin-2-ones was synthesized and evaluated as candidate antiinflammatory/analgesic agents as well as dual inhibitors of prostaglandin and leukotriene synthesis. Some compounds that showed dual inhibitory activity were found to possess equipotent antiinflammatory activities to indomethacin, with reduced
H.G. Lohr et al.
Chemische Berichte, 118, 914-914 (1985)
Michael Klein et al.
PloS one, 6(6), e20789-e20789 (2011-06-24)
Highly selective, cell-permeable and fast-acting inhibitors of individual kinases are sought-after as tools for studying the cellular function of kinases in real time. A combination of small molecule synthesis and protein mutagenesis, identified a highly potent inhibitor (1-Isopropyl-3-(phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine) of a
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