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Merck

128376

Sigma-Aldrich

对氟苯甲醛

98%

别名:

p-Fluorobenzaldehyde

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About This Item

线性分子式:
FC6H4CHO
CAS号:
分子量:
124.11
Beilstein:
385857
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

liquid

折射率

n20/D 1.521 (lit.)

bp

181 °C/758 mmHg (lit.)

mp

−10 °C (lit.)

密度

1.157 g/mL at 25 °C (lit.)

SMILES 字串

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

InChI

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

InChI 密鑰

UOQXIWFBQSVDPP-UHFFFAOYSA-N

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相关类别

應用

4-氟苯甲醛用于制备吡唑并吡啶UR-13756

訊號詞

Warning

危險分類

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

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

132.8 °F - closed cup

閃點(°C)

56 °C - closed cup

個人防護裝備

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
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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