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2,3,4-Trifluoronitrobenzene

99%

Synonim(y):

1,2,3-Trifluoro-4-nitrobenzene, 4-Nitro-1,2,3-trifluorobenzene

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Informacje o tej pozycji

Wzór liniowy:
F3C6H2NO2
Numer CAS:
Masa cząsteczkowa:
177.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-238-4
MDL number:
Assay:
99%
Form:
liquid


assay

99%

form

liquid

refractive index

n20/D 1.492 (lit.)

bp

92 °C/20 mmHg (lit.)

density

1.541 g/mL at 25 °C (lit.)

functional group

fluoro, nitro

SMILES string

[O-][N+](=O)c1ccc(F)c(F)c1F

InChI

1S/C6H2F3NO2/c7-3-1-2-4(10(11)12)6(9)5(3)8/h1-2H

InChI key

ARCACZWMYGILNI-UHFFFAOYSA-N

General description

2,3,4-Trifluoronitrobenzene is a fluoronitrobenzene and its biotransformation under methanogenic conditions has been studied by semicontinuous and batch tests.[1] 2,3,4-Trifluoronitrobenzene is an important pharmaceutical intermediate.

Application

2,3,4-Trifluoronitrobenzene was employed as starting reagent in the synthesis of ofloxacin. It was also used in the synthesis of the third generation quinolones antibacterial drugs.
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pictograms

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signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Klasa składowania

10 - Combustible liquids

wgk

WGK 3

flash_point_f

199.4 °F - closed cup

flash_point_c

93 °C - closed cup

ppe

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



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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów



Analytical profile of the fluoroquinolone antibacterials. I. Ofloxacin.
Okeri HA and Arhewoh IM.
African Journal of Biotechnology, 7(6) (2008)
Zhiqing Zhao et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 49(10), 1187-1197 (2014-05-23)
The fluorinated compounds are becoming a ubiquitous class of environmental contaminants because of their widespread applications, and their fate is a matter of great concern under anaerobic environment. In this work, the biotransformation of five fluoronitrobenzenes (FNBs), i.e., 2-fluoronitrobenzene (2-FNB)
Ultrasonic Promoted in Synthesis of 2, 3, 4-trichloronitrobenzene [J].
Yunqiang L and Guohui C.
Guangzhou Chemical Industry/ Guangzhou Huagong, 3, 024-024 (2009)



Numer pozycji handlu globalnego

SKUNUMER GTIN
338362-25G04061836826420

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