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Merck
CN

510246

Sigma-Aldrich

三氟棕榈酸甲酯

97%

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About This Item

线性分子式:
CF3COCO2CH3
CAS号:
分子量:
156.06
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

折射率

n20/D 1.332 (lit.)

沸点

86 °C (lit.)

密度

1.529 g/mL at 25 °C (lit.)

官能团

ester
fluoro
ketone

SMILES字符串

COC(=O)C(=O)C(F)(F)F

InChI

1S/C4H3F3O3/c1-10-3(9)2(8)4(5,6)7/h1H3

InChI key

XGLLQDIWQRQROJ-UHFFFAOYSA-N

一般描述

Methyl 3,3,3-trifluoropyruvate is an alkyl 3,3,3-trifluoropyruvate that can be synthesized using hexafluoropropene-1,2-oxide (HFPO) as a starting material. It reacts with aromatic amines, benzylic manoamines and diamines to form the corresponding hemiaminals.

应用

Methyl 3,3,3-trifluoropyruvate may be used in the synthesis of:
  • 2-hydroxy-2-trifluoromethylbutan-4-olides
  • 2-(trifluoromethyl)butan-4-olides
  • 4-trifluoromethyl-(2H)-pyridazin-3-ones
  • methyl 3-methoxy-2-trifluoromethylacrylate

象形图

Flame

警示用语:

Warning

危险声明

危险分类

Flam. Liq. 3

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

78.8 °F - closed cup

闪点(°C)

26 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Fluorinated butanolides and butenolides: Part 8. 2-(Trifluoromethyl) butan-4-olides by synthesis from methyl 3, 3, 3-trifluoropyruvate as building block.
Paleta O, et al.
Journal of Fluorine Chemistry, 111(2), 175-184 (2001)
Fluorinated butanolides and butenolides: Part 9. Synthesis of 2-(trifluoromethyl) butan-4-olides by Wittig reaction using methyl 3, 3, 3-trifluoropyruvate.
Palecek J, et al.
Journal of Fluorine Chemistry, 113(2), 177-183 (2002)
A convenient synthesis of 4-trifluoromethyl-(2H)-pyridazin-3-ones from methyl 3, 3, 3-trifluoropyruvate.
Sibgatulin DA, et al.
Synlett, 12, 1907-1911 (2005)
Methyl 3,3,3-trifluoropyruvate: an improved procedure starting from hexafluoropropene-1, 2-oxide; identification of byproducts.
Dolensky B, et al.
Journal of Fluorine Chemistry, 115(1), 67- 74 (2002)
Methyl 3, 3, 3-trifluoropyruvate hemiaminals: Stability and transaminations.
Dolensky B, et al.
Journal of Fluorine Chemistry, 126(5), 745-751 (2005)

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