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128376

Sigma-Aldrich

4-Fluorobenzaldehyde

98%

Sinónimos:

p-Fluorobenzaldehyde

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About This Item

Fórmula lineal:
FC6H4CHO
Número de CAS:
459-57-4
Peso molecular:
124.11
Beilstein/REAXYS Number:
385857
EC Number:
207-293-6
MDL number:
MFCD00003378
UNSPSC Code:
12352100
PubChem Substance ID:
24847852
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.521 (lit.)

bp

181 °C/758 mmHg (lit.)

mp

−10 °C (lit.)

density

1.157 g/mL at 25 °C (lit.)

functional group

aldehyde

SMILES string

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

InChI

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

InChI key

UOQXIWFBQSVDPP-UHFFFAOYSA-N

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Application

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

signalword

Warning

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

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

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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
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
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
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
Stephan Mokesch et al.
Frontiers in chemistry, 8, 209-209 (2020-04-23)
A series of 2-phenylbenzothiazole derivatives and their corresponding organometallic ruthenium(II) and osmium(II) complexes were synthesized, designed to exploit both, the attributes of the half-sandwich transition metal scaffold and the bioactivity spectrum of the applied 2-phenylbenzothiazoles. All synthesized compounds were characterized
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