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质量水平
方案
97%
表单
liquid
折射率
n20/D 1.469 (lit.)
沸点
178 °C (lit.)
密度
1.525 g/mL at 25 °C (lit.)
官能团
aldehyde
fluoro
SMILES字符串
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 key
YIRYOMXPMOLQSO-UHFFFAOYSA-N
一般描述
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.
应用
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.
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
165.2 °F - closed cup
闪点(°C)
74 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
Effects of aldehyde or dipyrromethane substituents on the reaction course leading to meso-substituted porphyrins.
Tetrahedron, 60(50), 11435-11444 (2004)
A new (R)-hydroxynitrile lyase from< i> Prunus mume</i>: asymmetric synthesis of cyanohydrins.
Tetrahedron, 61(46), 10908-10916 (2005)
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
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