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128376

Sigma-Aldrich

4-Fluorbenzaldehyd

98%

Synonym(e):

p-Fluorobenzaldehyde

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About This Item

Lineare Formel:
FC6H4CHO
CAS-Nummer:
459-57-4
Molekulargewicht:
124.11
Beilstein:
385857
EG-Nummer:
207-293-6
MDL-Nummer:
MFCD00003378
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24847852
NACRES:
NA.22

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.521 (lit.)

bp

181 °C/758 mmHg (lit.)

mp (Schmelzpunkt)

−10 °C (lit.)

Dichte

1.157 g/mL at 25 °C (lit.)

Funktionelle Gruppe

aldehyde

SMILES String

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

InChI

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

InChIKey

UOQXIWFBQSVDPP-UHFFFAOYSA-N

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Anwendung

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

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

132.8 °F - closed cup

Flammpunkt (°C)

56 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCP8592
MKCL4601
MKCK5020
MKCK5022
MKCK5023

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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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