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1-(2-Fluoro-5-nitrophenyl)ethan-1-one

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Products Intro: Product Name:1-(2-Fluoro-5-nitrophenyl)ethan-1-one
CAS:79110-05-7
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Products Intro: Product Name:2'-Fluoro-5'-Nitroacetophenone
CAS:79110-05-7
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CAS:79110-05-7
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CAS:79110-05-7
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CAS:79110-05-7
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1-(2-Fluoro-5-nitrophenyl)ethan-1-one manufacturers

1-(2-Fluoro-5-nitrophenyl)ethan-1-one Basic information
Product Name:1-(2-Fluoro-5-nitrophenyl)ethan-1-one
Synonyms:1-(2-Fluoro-5-nitrophenyl)ethan-1-one;2'-Fluoro-5'-nitroacetophenone 96%;1-(2-Fluoro-5-nitrophenyl)ethanone;1-(2-Fluoro-5-nitrophenyl)ethan-1-one, 3-Acetyl-4-fluoronitrobenzene;Ethanone,1-(2-fluoro-5-nitrophenyl)-;1-(2-Fluoro-5-nitrophenyl)ethan-1-one ISO 9001:2015 REACH;2'-FLUORO-5'-NITROACETOPHENONE
CAS:79110-05-7
MF:C8H6FNO3
MW:183.14
EINECS:639-356-2
Product Categories:Fluorine series
Mol File:79110-05-7.mol
1-(2-Fluoro-5-nitrophenyl)ethan-1-one Structure
1-(2-Fluoro-5-nitrophenyl)ethan-1-one Chemical Properties
Melting point 53-54 °C
Boiling point 241.0±20.0 °C(Predicted)
density 1.336±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
color White to Yellow to Green
InChIInChI=1S/C8H6FNO3/c1-5(11)7-4-6(10(12)13)2-3-8(7)9/h2-4H,1H3
InChIKeyBCXOSCQTHVTUET-UHFFFAOYSA-N
SMILESC(=O)(C1=CC([N+]([O-])=O)=CC=C1F)C
Safety Information
Hazard Codes Xi
HS Code 2914790090
MSDS Information
1-(2-Fluoro-5-nitrophenyl)ethan-1-one Usage And Synthesis
Uses2''-Fluoro-5''-nitroacetophenone
Synthesis
2'-Fluoroacetophenone

445-27-2

1-(2-Fluoro-5-nitrophenyl)ethan-1-one

79110-05-7

A solution of 1-(2-fluorophenyl)ethanone (90.0 g, 652 mmol) with fuming nitric acid (53.1 mL) in concentrated sulfuric acid (129 mL) was slowly added dropwise to concentrated sulfuric acid (360 mL, 93-98%) pre-cooled to -42 °C under mechanical stirring. The reaction mixture was kept stirred at -42°C for 30 minutes. Upon completion of the reaction, the mixture was slowly poured into ice (1.3 kg) to quench the reaction. Subsequently, water (1 L) was added to precipitate the product from the solution. After all the ice melted, the precipitate was collected by filtration. The resulting solid was dissolved in EtOAc and the organic layer was washed sequentially with 5% aqueous Na2CO3 (2 x 300 mL), water (1 x 300 mL) and brine (1 x 300 mL), dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated to give a yellow solid 1-(2-fluoro-5-nitrophenyl)ethanone (115 g, 97% yield).

References[1] Patent: WO2012/139425, 2012, A1. Location in patent: Page/Page column 117
[2] Patent: WO2011/44184, 2011, A1. Location in patent: Page/Page column 99-100
[3] Patent: US2004/122237, 2004, A1. Location in patent: Page 388
[4] Journal of Heterocyclic Chemistry, 1991, vol. 28, # 3, p. 673 - 683
[5] Patent: US2002/151715, 2002, A1
1-(2-Fluoro-5-nitrophenyl)ethan-1-one Preparation Products And Raw materials
Raw materials2'-Fluoroacetophenone
Preparation Products3-METHYL-1H-INDAZOL-5-AMINE-->2-Propanesulfinamide, N-[1-(2-fluoro-5-nitrophenyl)ethylidene]-2-methyl-, [N(E),S(R)]-
Tag:1-(2-Fluoro-5-nitrophenyl)ethan-1-one(79110-05-7) Related Product Information
1,2,3-Trifluoro-4-nitrobenzene 1-Fluoro-3-nitrobenzene BENZENEPROPANENITRILE, 2,4-DIFLUORO-5-NITRO-B-OXO- 2-Fluoro-5-nitrobenzaldehyde 2-Fluoro-5-nitrotoluene 1-(2-Fluoro-5-nitrophenyl)ethan-1-one

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