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5-Fluoro-2-nitro-N-phenylaniline is a specialty chemical compound with the formula C12H9FN2O2. It is typically found in the form of an off-white powder and is known for its unique properties, including a relatively high molecular weight of 238.21 g/mol and a melting point range of 49-51°C. 5-Fluoro-2-nitro-N-phenylaniline is primarily utilized for industrial and research purposes.

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  • 322-68-9 Structure
  • Basic information

    1. Product Name: 5-Fluoro-2-nitro-N-phenylaniline
    2. Synonyms: 5-Fluoro-2-nitro-N-phenylaniline
    3. CAS NO:322-68-9
    4. Molecular Formula: C12H9FN2O2
    5. Molecular Weight: 232.2104632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 322-68-9.mol
  • Chemical Properties

    1. Melting Point: 93-94 °C
    2. Boiling Point: 343.6±32.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.353±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: -4.30±0.50(Predicted)
    10. CAS DataBase Reference: 5-Fluoro-2-nitro-N-phenylaniline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-Fluoro-2-nitro-N-phenylaniline(322-68-9)
    12. EPA Substance Registry System: 5-Fluoro-2-nitro-N-phenylaniline(322-68-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 322-68-9(Hazardous Substances Data)

322-68-9 Usage

Uses

Used in Chemical Synthesis:
5-Fluoro-2-nitro-N-phenylaniline is used as an intermediate in the synthesis of various organic compounds. Its unique structure and properties make it a valuable building block for the creation of new molecules with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-Fluoro-2-nitro-N-phenylaniline is used as a research compound for the development of new drugs. Its chemical properties allow it to be a potential candidate for the treatment of various diseases, and it can be further modified to improve its therapeutic effects.
Used in Material Science:
5-Fluoro-2-nitro-N-phenylaniline is used as a component in the development of new materials with specific properties. Its incorporation into materials can lead to improved performance in areas such as electronics, coatings, and adhesives.
Used in Dye and Pigment Production:
In the dye and pigment industry, 5-Fluoro-2-nitro-N-phenylaniline is used as a starting material for the production of various dyes and pigments. Its chemical structure contributes to the color and stability of the final products, making it an important component in this field.
Used in Analytical Chemistry:
5-Fluoro-2-nitro-N-phenylaniline is used as a reference compound in analytical chemistry for the calibration of instruments and the development of new analytical methods. Its distinct properties make it a reliable standard for comparison and measurement.

Check Digit Verification of cas no

The CAS Registry Mumber 322-68-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 322-68:
(5*3)+(4*2)+(3*2)+(2*6)+(1*8)=49
49 % 10 = 9
So 322-68-9 is a valid CAS Registry Number.

322-68-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Fluoro-2-nitro-N-phenylaniline

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:322-68-9 SDS

322-68-9Relevant articles and documents

An Organic Zeolite With 10 ? Diameter Pores Assembles From a Soluble and Flexible Building Block by Non-Covalent Interactions

Plater, M. John,Harrison, William T. A.

, p. 457 - 463 (2019)

Two similar molecular building blocks, which both contain a hydrogen-bonded nitro group, have been prepared and crystallised. One structure has more flexibility with a butyl side chain which allows an open framework organic zeolite to form with large 10 ?

Design, Synthesis, and Antifungal Activities of Novel Aromatic Carboxamides Containing a Diphenylamine Scaffold

Zhang, Aigui,Yue, Ying,Yang, Jian,Shi, Jiaxing,Tao, Ke,Jin, Hong,Hou, Taiping

, (2019/05/08)

A series of novel N-(2-(phenylamino)-4-fluorophenyl)-pyrazole-4-carboxamides 1-15 and aromatic carboxamides with a diphenylamine scaffold 16-29 were designed, synthesized, and evaluated for their antifungal activities. In vitro experiments showed that com

Design, Synthesis, and Antifungal Activities of Novel Aromatic Carboxamides Containing a Diphenylamine Scaffold

Zhang, Aigui,Yue, Ying,Yang, Jian,Shi, Jiaxing,Tao, Ke,Jin, Hong,Hou, Taiping

, p. 5008 - 5016 (2019/05/08)

A series of novel N-(2-(phenylamino)-4-fluorophenyl)-pyrazole-4-carboxamides 1-15 and aromatic carboxamides with a diphenylamine scaffold 16-29 were designed, synthesized, and evaluated for their antifungal activities. In vitro experiments showed that com

A heterocyclic ligands containing compounds and methods for their preparation, application (by machine translation)

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Paragraph 0153; 0154; 0155; 0156; 0157, (2016/10/08)

The present invention provides a compound containing heterocyclic ligands and its preparation method, an electroluminescent device. The present invention provides heterocycle-containing ligand compound, through the particular selection of heterocyclic ligands and different metal binding, can adjust the wavelength of the compound, the organic metal compound used in the organic electroluminescent device, to make the device light-emitting efficiency is improved, and the service life is long. (by machine translation)

Compound with heterocyclic ligand and preparation method and application thereof

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Paragraph 0106; 0107; 0108; 0109, (2016/10/08)

The invention provides a compound with a heterocyclic ligand and a preparation method and application thereof. According to the compound with the heterocyclic ligand, the specific heterocyclic ligand is selected to be combined with metal aluminum, so that after the obtained organic compound is applied to an organic light-emitting device, the light-emitting efficiency of the device is improved, and the service life is long.

Lithium compound with heterocyclic ligand and preparation method and application thereof

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Paragraph 0120; 0121; 0122; 0123; 0124, (2016/10/08)

The invention provides a lithium compound with a heterocyclic ligand and a preparation method and application thereof. According to the lithium compound with the heterocyclic ligand, the specific heterocyclic ligand is selected to be combined with metal lithium, so that after the obtained organic lithium compound is applied to an organic light-emitting device, the light-emitting efficiency of the device is improved, and the service life is long.

Oxidative nucleophilic aromatic amination of nitrobenzenes

Khutorianskyi,Sonawane,Po?ta,Klepetá?ová,Beier

supporting information, p. 7237 - 7240 (2016/06/09)

Nitrobenzenes substituted with electron-acceptor groups such as halogen, nitro, trifluoromethyl, pentafluorosulfanyl, or cyano underwent oxidative nucleophilic substitution with lithium salts of arylamines to afford N-aryl-2-nitroanilines.

A paddle-wheel motif versus an extended network: Two crystalline forms of 2,4-bis(phenylamino)nitrobenzene

Plater, M. John,Harrison, William T.A.

, p. 98 - 104 (2015/06/16)

2,4-Difluoronitrobenzene is reacted with either one or two amines selected from aniline, ammonia, butylamine and benzylamine. All products are characterised spectroscopically and by single-crystal structure determinations. When formed as a minor component

HETEROCYCLIC COMPOUNDS AND METHODS OF USE

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Page/Page column 116, (2012/08/27)

Formula I compounds, including stereoisomers, geometric isomers, tautomers, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting the delta isoform of PI3K, and for treating disorders mediated by lipid kinases such as inflammation, immunological disorders, and cancer. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

Novel 1,5-benzodiazepines as CCK-B ligands. Effect of aryl-carbamic substituents at the C-3 position together with halogen substitution on the benzo-fused ring

Tranquillini, M. Elvira,Cassara, Paolo G.,Corsi, Mauro,Curotto, Giovanni,Donati, Daniele,Finizia, Gabriella,Pentassuglia, Giorgio,Polinelli, Stefano,Tarzia, Giorgio,Ursini, Antonella,Van Amsterdam, Franciscus T.M.

, p. 353 - 357 (2007/10/03)

The synthesis and biological evaluation as potential CCK-B receptor ligands of a number of 1-isopentyl-3-aryloxycarbamoyl-5-aryl-1,5-benzodiazepines substituted with halogen atoms on the benzo-fused ring is here briefly discussed.

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