128376
4-Fluorobenzaldehyde
98%
Sinónimos:
p-Fluorobenzaldehyde
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Acerca de este artículo
Fórmula lineal:
FC6H4CHO
Número CAS:
Peso molecular:
124.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-293-6
Beilstein/REAXYS Number:
385857
MDL number:
Assay:
98%
Form:
liquid
Servicio técnico
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Permítanos ayudarleQuality Level
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, fluoro
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
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 3
Clase de almacenamiento
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
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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