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162531

Sigma-Aldrich

3-Fluorobenzoyl chloride

98%

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About This Item

Formula condensata:
FC6H4COCl
Numero CAS:
1711-07-5
Peso molecolare:
158.56
Beilstein:
636610
Numero CE:
216-977-3
Numero MDL:
MFCD00000670
Codice UNSPSC:
12352100
ID PubChem:
24849988
NACRES:
NA.22

Saggio

98%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.529 (lit.)

P. eboll.

189 °C (lit.)

Punto di fusione

−30 °C (lit.)

Densità

1.304 g/mL at 25 °C (lit.)

Stringa SMILE

Fc1cccc(c1)C(Cl)=O

InChI

1S/C7H4ClFO/c8-7(10)5-2-1-3-6(9)4-5/h1-4H
SYVNVEGIRVXRQH-UHFFFAOYSA-N

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Applicazioni

3-Fluorobenzoyl chloride was used in synthesis of 4-[18F]fluoro-N-[2-[1-(2-methoxyphenyl)-1-piperazinyl]ethyl-N-2-pyridinyl-benzamide by radiosynthesis. It was also used as reagent in one-pot synthesis of N-(1,3-diphenyl-1H-pyrazol-5-yl)amides. It was used in three phase hollow fiber liquid-phase microextraction with in situ derivatization method coupled with HPLC-UV for the determination of metformin hydrochloride in biological fluids.

Pittogrammi

Corrosion
GHS05

Avvertenze

Danger

Indicazioni di pericolo

H314

Classi di pericolo

Eye Dam. 1 - Skin Corr. 1B

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

179.6 °F - closed cup

Punto d’infiammabilità (°C)

82 °C - closed cup

Dispositivi di protezione individuale

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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An efficient one-pot synthesis of N-(1, 3-diphenyl-1H-pyrazol-5-yl) amides.
Su W-N, et al.
Journal of Heterocyclic Chemistry, 47(4), 831-837 (2010)
D Le Bars et al.
Nuclear medicine and biology, 25(4), 343-350 (1998-06-25)
No-carrier-added 4-[18F]fluoro-N-[2-[1-(2-methoxyphenyl)-1 piperazinyl]ethyl-N-2-pyridinyl-benzamide (p-[18F]MPPF) was synthesized by nucleophilic substitution of the corresponding nitro compound in the presence of Kryptofix 222 and K2CO3 by microwave heating (3 min, 500 W) using a remotely controlled radiosynthesis. Baseline separation of p-[18F]MPPF from the
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Phosphoinositide 3-kinase α (PI3Kα) has emerged as a promising target for anticancer drug design. Target compounds were designed to investigate the effect of the p-OCH3 motifs on ligand/PI3Kα complex interaction and antiproliferative activity. Synthesis of the proposed compounds, biological examination
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Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 941, 123-130 (2013-11-10)
A three phase hollow fiber liquid-phase microextraction with in situ derivatization (in situ HF-LPME) followed by high-performance liquid chromatography-ultraviolet detection (HPLC-UV) method was developed for the trace determination of metformin hydrochloride (MH) in biological fluids. A new derivatization agent pentafluorobenzoyl

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