128376
对氟苯甲醛
98%
别名:
p-Fluorobenzaldehyde
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关于此项目
线性分子式:
FC6H4CHO
化学文摘社编号:
分子量:
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
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
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-氟苯甲醛，又称对氟苯甲醛，一种有机化合物，常用于缩合反应合成酚类单体。
Application
4-氟苯甲醛用于制备吡唑并吡啶UR-13756。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 3
存储类别
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
法规信息
危险化学品
此项目有
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
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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
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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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