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CAS

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330-89-2

4-Fluoro-4'-nitrodiphenylamine is an organic compound with the chemical formula C12H9FN2O2. It is a derivative of diphenylamine, featuring a fluorine atom at the 4-position and a nitro group at the 4'-position. This yellow crystalline solid is primarily used as an antioxidant and stabilizer in various industrial applications, such as rubber and plastic manufacturing, to prevent degradation caused by heat, light, and oxygen exposure. Due to its chemical structure, it exhibits excellent thermal and oxidative stability, making it a valuable additive in the production of materials that require resistance to aging and environmental stress.

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  • 330-89-2 Structure

  • Basic information

    1. Product Name: 4-Fluoro-4'-nitrodiphenylamine
    2. Synonyms: 4-Fluoro-4'-nitrodiphenylamine
    3. CAS NO:330-89-2
    4. Molecular Formula: C12H9FN2O2
    5. Molecular Weight: 232.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 330-89-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Fluoro-4'-nitrodiphenylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Fluoro-4'-nitrodiphenylamine(330-89-2)
    11. EPA Substance Registry System: 4-Fluoro-4'-nitrodiphenylamine(330-89-2)

  • 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: 330-89-2(Hazardous Substances Data)

330-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 330-89-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 330-89:
(5*3)+(4*3)+(3*0)+(2*8)+(1*9)=52
52 % 10 = 2
So 330-89-2 is a valid CAS Registry Number.

330-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-N-(4-nitrophenyl)aniline

1.2 Other means of identification

Product number -
Other names (4-fluoro-phenyl)-(4-nitro-phenyl)-amine

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:330-89-2 SDS

330-89-2Downstream Products

330-89-2Relevant articles and documents

Diarylamine Synthesis via Desulfinylative Smiles Rearrangement

Sephton, Thomas,Large, Jonathan M.,Butterworth, Sam,Greaney, Michael F.

, p. 1132 - 1135 (2022/02/09)

Diarylamines are obtained directly from sulfinamides through a novel rearrangement sequence. The transformation is transition metal-free and proceeds under mild conditions, providing facile access to highly sterically hindered diarylamines that are otherw

Ligand-Enabled Gold-Catalyzed C(sp2)-N Cross-Coupling Reactions of Aryl Iodides with Amines

Akram, Manjur O.,Das, Avishek,Chakrabarty, Indradweep,Patil, Nitin T.

supporting information, p. 8101 - 8105 (2019/10/11)

The first example of ancillary (P,N)-ligand-enabled gold-catalyzed C-N cross-coupling reactions of aryl iodides with amines is reported. The high generality of the reaction in de novo synthesis, late-stage modifications, and cascade processes to access functionalized indolinones and carbazoles underscores the synthetic potential of the presented strategy. Monitoring the reaction with ESI-HRMS and NMR provided strong evidence for the in situ formation of putative high valent Au(III) intermediates.

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