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Merck

529184

Sigma-Aldrich

2,4,5-三氟苯甲醛

97%

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About This Item

线性分子式:
F3C6H2CHO
分子量:
160.09
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

折射率

n20/D 1.482 (lit.)

bp

168 °C (lit.)

密度

1.408 g/mL at 25 °C (lit.)

官能基

aldehyde
fluoro

SMILES 字串

Fc1cc(F)c(C=O)cc1F

InChI

1S/C7H3F3O/c8-5-2-7(10)6(9)1-4(5)3-11/h1-3H

InChI 密鑰

CYIFJRXFYSUBFW-UHFFFAOYSA-N

相关类别

應用

2,4,5-Trifluorobenzaldehyde may be used in the synthesis of:
  • bis(2,4,5-trifluorophenyl)methanone
  • 8-phenyl-7-tosyl-1-(2,4,5-trifluorophenyl)octahydro-1H-pyrano[3,4-c] pyridine
  • (E)-4-methoxy-N′-(2,4,5-trifluorobenzylidene)-benzohydrazide monohydrate

象形圖

FlameExclamation mark

訊號詞

Warning

危險分類

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

138.2 °F - closed cup

閃點(°C)

59 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析证书(COA)

Lot/Batch Number

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Zachary R Woydziak et al.
Synthesis, 46(2), 158-164 (2014-06-11)
Fluorinated fluorophores are valuable tools for studies of biological systems. However, amine-reactive single-isomer derivatives of these compounds are often very expensive. To provide an inexpensive alternative, we report a practical synthesis of 4-carboxy-Pennsylvania Green methyl ester. Derivatives of this hydrophobic
(E)-4-Methoxy-N'-(2, 4, 5-trifluorobenzylidene) benzohydrazide monohydrate.
Maheswari R, et al.
IUCrJ, 1(5), x160846-x160846 (2016)
Aminol initiated Prins cyclization for the synthesis of octahydro-1H-pyrano [3, 4-c] pyridine and hexahydro-1H-furo [3, 4-c] pyrrole derivatives.
Tetrahedron Letters, 55(34), 4817-4821 (2014)
Zachary R Woydziak et al.
The Journal of organic chemistry, 77(1), 473-481 (2011-11-25)
Fluorination of fluorophores can substantially enhance their photostability and improve spectroscopic properties. To facilitate access to fluorinated fluorophores, bis(2,4,5-trifluorophenyl)methanone was synthesized by treatment of 2,4,5-trifluorobenzaldehyde with a Grignard reagent derived from 1-bromo-2,4,5-trifluorobenzene, followed by oxidation of the resulting benzyl alcohol.

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