426016
4,4,4-三氟-1-（2-呋喃基）-1,3-丁二酮
99%
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C8H5F3O3
化学文摘社编号:
分子量:
206.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
206-315-1
MDL number:
Assay:
99%
Form:
liquid
InChI key
OWLPCALGCHDBCN-UHFFFAOYSA-N
InChI
1S/C8H5F3O3/c9-8(10,11)7(13)4-5(12)6-2-1-3-14-6/h1-3H,4H2
SMILES string
FC(F)(F)C(=O)CC(=O)c1ccco1
assay
99%
form
liquid
refractive index
n20/D 1.528 (lit.)
bp
203 °C (lit.)
mp
19-21 °C (lit.)
density
1.391 g/mL at 25 °C (lit.)
functional group
fluoro, ketone
storage temp.
2-8°C
Quality Level
General description
4,4,4-三氟-1-(2-呋喃基)-1,3-丁二酮（呋喃基三氟丙酮，FTFA）为β-二酮。对体外培养的肿瘤细胞和正常细胞进行了细胞毒活性评价。研究表明，4,4,4-三氟-1-(2-呋喃基)-1,3-丁二酮能部分抑制ETP（电子传递粒子，从牛肉心脏线粒体分离）中亚铁氰化物的氧化。 研究了它与N,N,N′,N′-四甲基烷基二胺的反应形成离子加合物。本文报道了烯醇和酮两种形式的超疏水脂肪酸的构象分析。
Application
4,4,4-三氟-1-(2-呋喃基)-1,3-丁二酮(tfa)可用于以下研究：
- 在[Eu(tfa)3]2bpm络合物(bpm=2,2′-二嘧啶)的合成中作为封顶配体。
- 在[13CD2]苄胺的多步合成中用作试剂。
- 作为合成3-三氟甲基-2-芳基羰基喹啉1,4-di-N-氧化物衍生物的试剂，与相应的苯并呋咱氧化物反应。
- 在全氟烷基取代唑的有效合成中。
- 2-芳基羰基-3-三氟甲基喹啉1,4-di-N-氧化物衍生物的合成。
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
188.6 °F - closed cup
flash_point_c
87 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Kensuke Nakano et al.
Anticancer research, 24(2B), 711-717 (2004-05-27)
A variety of beta-diketones were evaluated for their cytotoxic profiles against oral human normal and tumor cells. Among 22 compounds (BD1-22) tested, the cytotoxicity of 3-formylchromone (BD17) (CC50=7.8 microg/mL) against human oral squamous cell carcinoma (HSC-2) cells was higher than
Topography of the cristae membrane as elucidated by a new inhibitor, trifluorofurylbutanedione.
H J Harmon et al.
Biochemical and biophysical research communications, 55(1), 169-173 (1973-11-01)
Acyclic tertiary diamines and 1, 4, 7,10-tetraazacyclododecane with fluorine-containing β-diketones: Leading to low melting ionic adducts.
Gupta OD, et al.
Journal of Fluorine Chemistry, 126(8), 1222-1229 (2005)
Synthesis and biological evaluation of new 2-arylcarbonyl-3-trifluoromethylquinoxaline 1,4-di-N-oxide derivatives and their reduced analogues.
Solano B, et al.
Journal of Medicinal Chemistry, 50(22), 5485-5492 (2007)
Adoración Marin et al.
Experimental parasitology, 118(1), 25-31 (2007-07-07)
Derivatives of 3-trifluoromethyl-2-arylcarbonylquinoxaline 1,4-di-N-oxide (4b-g, 5b-g, 6a-g) were synthesized and evaluated for their capacity to inhibit the growth of chloroquine-resistant Plasmodium falciparum FCB1 strain in culture. Compound 7-chloro-2-(2-furylcarbonyl)-3-trifluoromethyl-1,4-quinoxaline di-N-oxide (5g) was the most active being almost 5 times more active
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持