510254
3,3,3-三氟丙酮酸乙酯
97%
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关于此项目
线性分子式:
CF3COCO2C2H5
化学文摘社编号:
分子量:
170.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2087388
产品名称
3,3,3-三氟丙酮酸乙酯, 97%
InChI
1S/C5H5F3O3/c1-2-11-4(10)3(9)5(6,7)8/h2H2,1H3
SMILES string
CCOC(=O)C(=O)C(F)(F)F
InChI key
KJHQVUNUOIEYSV-UHFFFAOYSA-N
assay
97%
refractive index
n20/D 1.341 (lit.)
n/D (lit.)
density
1.283 g/mL at 25 °C (lit.)
functional group
ester
fluoro
ketone
Quality Level
Application
3,3,3-三氟丙酮酸乙酯可用于制备 N-杂芳基(三氟甲基)羟基链烷酸酯。
General description
3,3,3-三氟丙酮酸乙酯是一种三氟甲基化化合物。已有研究报道了在不同反应条件下，简单酚和吲哚与3,3,3-三氟丙酮酸乙酯的不对称Friedel-Crafts烷基化反应。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
87.8 °F - closed cup
flash_point_c
31 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
Novel Enantiocomplementary C2-Symmetric Chiral Bis (imidazoline) Ligands: Highly Enantioselective Friedel?Crafts Alkylation of Indoles with Ethyl 3, 3, 3-Trifluoropyruvate.
Nakamura S, et al.
Advanced Synthesis & Catalysis, 350(10), 1443-1448 (2008)
Organocatalytic enantioselective Friedel?Crafts alkylation of simple phenols with trifluoropyruvate.
Zhao JL, et al.
Tetrahedron Letters, 49(9), 1476-1479 (2008)
Synthesis of N-Heteroaryl (trifluoromethyl) hydroxyalkanoic Acid Esters by Highly Efficient Solid Acid-Catalyzed Hydroxyalkylation of Indoles and Pyrroles with Activated Trifluoromethyl Ketones.
Abid M and Torok B.
Advanced Synthesis & Catalysis, 347(14), 1797-1803 (2005)
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