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Merck
CN

128376

4-Fluorobenzaldehyde

98%

Synonym(s):

p-Fluorobenzaldehyde

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About This Item

Linear Formula:
FC6H4CHO
CAS Number:
459-57-4
Molecular Weight:
124.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847852
EC Number:
207-293-6
Beilstein/REAXYS Number:
385857
MDL number:
MFCD00003378
Assay:
98%
Form:
liquid

Key Documents

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InChI key

UOQXIWFBQSVDPP-UHFFFAOYSA-N

InChI

1S/C7H5FO/c8-7-3-1-6(5-9)2-4-7/h1-5H

SMILES string

[H]C(=O)c1ccc(F)cc1

assay

98%

form

liquid

Quality Level

100

bp

181 °C/758 mmHg (lit.)

mp

−10 °C (lit.)

density

1.157 g/mL at 25 °C (lit.)

functional group

aldehyde, fluoro

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General description

4-Fluorobenzaldehyde, also known as p-Fluorobenzaldehyde is an organic compound often used in the condensation reactions for the synthesis of phenolic monomers.

Application

4-Fluorobenzaldehyde was used in the preparation of pyrazolopyridine UR-13756.

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

132.8 °F - closed cup

flash_point_c

56 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
MKDB0687
0000488085
0000488085
0000483853
0000483853

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Abdul Hafeez et al.
Polymers, 11(9) (2019-09-22)
Bis-aldehyde monomers 4-(4'-formyl-phenoxy)benzaldehyde (3a), 3-methoxy-4-(4'-formyl-phenoxy)benzaldehyde (3b), and 3-ethoxy-4-(4'-formyl-phenoxy)benzaldehyde (3c) were synthesized by etherification of 4-fluorobenzaldehyde (1) with 4-hydroxybenzaldehyde (2a), 3-methoxy-4-hydroxybenzaldehyde (2b), and 3-ethoxy-4-hydroxybenzaldehyde (2c), respectively. Each monomer was polymerized with p-phenylenediamine and 4,4'-diaminodiphenyl ether to yield six poly(azomethine)s. Single crystal
Mark C Bagley et al.
Future medicinal chemistry, 2(2), 193-201 (2011-03-24)
UR-13756 is a potent and selective p38 mitogen-activated protein kinase (MAPK) inhibitor, reported to have good bioavailability and pharmacokinetic properties and, thus, is of potential use in the treatment of accelerated aging in Werner syndrome. Irradiation of 2-chloroacrylonitrile and methylhydrazine
Xuemei Tian et al.
Enzyme and microbial technology, 84, 32-40 (2016-02-02)
The first Novozym 435 lipase-catalyzed Morita-Baylis-Hillman (MBH) reaction with amides as co-catalyst was realized. Results showed that neither Novozym 435 nor amide can independently catalyze the reaction. This co-catalytic system that used a catalytic amount of Novozym 435 with a
Ana Margarida Araújo et al.
Archives of toxicology, 92(11), 3307-3323 (2018-09-27)
3,4-Methylenedioxymethamphetamine (MDMA, ecstasy) is a well-known hepatotoxic drug. Although its toxicity has been thoroughly studied at high concentrations, there is still insufficient knowledge on possible alterations of cell function at subtoxic concentrations, which are in fact more representative concentrations of
Bin-Yu Wen et al.
Journal of Asian natural products research, 21(7), 702-715 (2019-01-01)
Desmosdumotin C (Des C), a natural product isolated from the roots of Desmos dumosus, has shown good antitumor activity. A three dimensional quantitative structure-activity relationship (QSAR) study using the comparative molecular field analysis (CoMFA) method was performed on 32 Des
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