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348074

Sigma-Aldrich

2-氯-4-氟苯甲醛

97%

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5 G
$63.40

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5 G
$63.40

About This Item

线性分子式:
ClC6H3(F)CHO
CAS号:
84194-36-5
分子量:
158.56
MDL编号:
MFCD00042527
UNSPSC代码:
12352100
PubChem化学物质编号:
24861548
NACRES:
NA.22

$63.40

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质量水平

100

方案

97%

表单

solid

沸点

118-120 °C/50 mmHg (lit.)

mp

60-63 °C (lit.)

官能团

aldehyde
chloro
fluoro

SMILES字符串

Fc1ccc(C=O)c(Cl)c1

InChI

1S/C7H4ClFO/c8-7-3-6(9)2-1-5(7)4-10/h1-4H

InChI key

KMQWNQKESAHDKD-UHFFFAOYSA-N

相关类别

一般描述

2-Chloro-4-fluorobenzaldehyde is a halogen substituted benzaldehyde.

应用

2-Chloro-4-fluorobenzaldehyde may be used in the synthesis of substituted α-cyanocinnamic acid, via Knoevenagel condensation reaction.[1] It may be used in the synthesis of 2-(2-benzimidazolyl)-3-(2-chloro-4-fluorophenyl)acrylonitrile.[2]

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

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

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCM3754
MKCK3916
MKCF1747
MKCB0381V
MKBS0478V

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Biological activity and DNA binding studies of 2-substituted benzimidazo [1, 2-a] quinolines bearing different amino side chains.
Perin N, et al.
MedChemComm, 4(12), 1537-1550 (2013)
Thorsten W Jaskolla et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(34), 12200-12205 (2008-08-30)
Matrix-assisted laser desorption ionization (MALDI) has become an enabling technology for the fields of protein mass spectrometry (MS) and proteomics. Despite its widespread use, for example, in protein identification via peptide mass fingerprinting, a comprehensive model for the generation of

商品

Knoevenagel Condensation Reaction

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

相关内容

Knoevenagel Condensation Reaction

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

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