추천 제품
분석
97%
refractive index
n20/D 1.332 (lit.)
bp
86 °C (lit.)
density
1.529 g/mL at 25 °C (lit.)
SMILES string
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
일반 설명
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.
애플리케이션
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
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Fluorinated butanolides and butenolides: Part 8. 2-(Trifluoromethyl) butan-4-olides by synthesis from methyl 3, 3, 3-trifluoropyruvate as building block.
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.
Journal of Fluorine Chemistry, 113(2), 177-183 (2002)
Methyl 3,3,3-trifluoropyruvate: an improved procedure starting from hexafluoropropene-1, 2-oxide; identification of byproducts.
Journal of Fluorine Chemistry, 115(1), 67- 74 (2002)
A convenient synthesis of 4-trifluoromethyl-(2H)-pyridazin-3-ones from methyl 3, 3, 3-trifluoropyruvate.
Synlett, 12, 1907-1911 (2005)
Methyl 3, 3, 3-trifluoropyruvate hemiaminals: Stability and transaminations.
Journal of Fluorine Chemistry, 126(5), 745-751 (2005)
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