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Merck
CN

328936

Sigma-Aldrich

2,3,5,6-四氟苯甲醛

97%

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关于此项目

线性分子式:
HC6F4CHO
化学文摘社编号:
分子量:
178.08
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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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.

象形图

Exclamation mark

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

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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)
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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