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化驗
97%
形狀
liquid
折射率
n20/D 1.469 (lit.)
bp
178 °C (lit.)
密度
1.525 g/mL at 25 °C (lit.)
SMILES 字串
Fc1cc(F)c(F)c(C=O)c1F
InChI
1S/C7H2F4O/c8-4-1-5(9)7(11)3(2-12)6(4)10/h1-2H
InChI 密鑰
YIRYOMXPMOLQSO-UHFFFAOYSA-N
一般說明
2,3,5,6-Tetrafluorobenzaldehyde is a polysubstituted benzaldehyde and was evaluated as a substrate of PmHNL (Prunus mume hydroxynitrile lyase). Reaction of 2,3,5,6-tetrafluorobenzaldehyde with dipyrromethane was reported.
應用
2,3,5,6-Tetrafluorobenzaldehyde was used in the preparation of 1,3-bis(2,4,6-trimethylphenyl)-2-(2,3,5,6-tetrafluorophenyl)imidazolidine and 1,3-dimethyl-2-(2,3,5,6-tetrafluorophenyl)imidazolidine.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
165.2 °F - closed cup
閃點（°C）
74 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Effects of aldehyde or dipyrromethane substituents on the reaction course leading to meso-substituted porphyrins.
Geier III, et al.
Tetrahedron, 60(50), 11435-11444 (2004)
Gregory W Nyce et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 10(16), 4073-4079 (2004-08-19)
The synthesis of N-heterocyclic carbene (NHC) adducts by condensation of diamines with appropriately substituted benzaldehydes is described. This simplified approach provides the NHC adduct without first having to generate the carbene followed by its protection. These adducts undergo thermal deprotection
A new (R)-hydroxynitrile lyase from< i> Prunus mume</i>: asymmetric synthesis of cyanohydrins.
Nanda S, et al.
Tetrahedron, 61(46), 10908-10916 (2005)
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