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CAS

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155310-23-9

2-Fluoro-5-methyldiphenylamine is a chemical compound with the molecular formula C13H12FN. It is an aromatic amine that contains a fluorine and a methyl group attached to a diphenylamine core.
Used in Pharmaceutical Industry:
2-Fluoro-5-methyldiphenylamine is used as a chemical intermediate for the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds.
Used in Agrochemical Industry:
2-Fluoro-5-methyldiphenylamine is used as a building block in the synthesis of agrochemicals, playing a role in the development of agricultural products.
Used in Dye Industry:
2-Fluoro-5-methyldiphenylamine is used as a chemical intermediate in the production of dyes, contributing to the creation of colorants for various applications.
Used in Polymer Synthesis:
2-Fluoro-5-methyldiphenylamine is used as a monomer or building block in the synthesis of organic materials such as polymers, enhancing their properties and performance.
Used in Organic Reactions:
2-Fluoro-5-methyldiphenylamine is used as a reagent in organic reactions, facilitating specific chemical transformations and processes.
Used in Metal Extraction and Separation Processes:
2-Fluoro-5-methyldiphenylamine is used for forming stable and selective complexes with certain metal ions, making it useful in metal extraction and separation processes.
It is important to handle 2-Fluoro-5-methyldiphenylamine with proper safety precautions due to its potential hazards if not handled carefully.

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  • 155310-23-9 Structure

  • Basic information

    1. Product Name: 2-Fluoro-5-methyldiphenylamine
    2. Synonyms: 2-Fluoro-5-methyldiphenylamine
    3. CAS NO:155310-23-9
    4. Molecular Formula: C13H12FN
    5. Molecular Weight: 201.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 155310-23-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 283.7°C at 760 mmHg
    3. Flash Point: 125.4°C
    4. Appearance: /
    5. Density: 1.143g/cm3
    6. Vapor Pressure: 0.00312mmHg at 25°C
    7. Refractive Index: 1.603
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-Fluoro-5-methyldiphenylamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Fluoro-5-methyldiphenylamine(155310-23-9)
    12. EPA Substance Registry System: 2-Fluoro-5-methyldiphenylamine(155310-23-9)

  • 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: 155310-23-9(Hazardous Substances Data)

155310-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155310-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,3,1 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 155310-23:
(8*1)+(7*5)+(6*5)+(5*3)+(4*1)+(3*0)+(2*2)+(1*3)=99
99 % 10 = 9
So 155310-23-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H12FN/c1-10-7-8-12(14)13(9-10)15-11-5-3-2-4-6-11/h2-9,15H,1H3

155310-23-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-5-methyl-N-phenylaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,2-fluoro-5-methyl-N-phenyl

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:155310-23-9 SDS

155310-23-9Downstream Products

155310-23-9Relevant articles and documents

Emissive monomeric metal complexes

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Page/Page column 4-5, (2010/11/30)

Monomeric metal complexes having improved luminescence properties are provided. In one embodiment, a monomeric metal complex is represented by the formula [PN]M(L)2. PN is an amidophosphine ligand, and M may be any metal capable of exhibiting l

Process for producing diphenylamines or N,N'-diphenyl-phenylenediamines

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, (2008/06/13)

Diphenylamines or N,N'-diphenyl-phenylenediamines can be obtained by heat-reacting an aniline or a phenylenediamine with preferably an excess of a phenol in an amount of 4 to 20 moles per mole of the aniline or phenylenediamine in the presence of a hydrogen transfer catalyst and a cyclohexanone corresponding to said phenol. The excess phenol used in the reaction undergoes reduction in the reaction system to form a cyclohexanone, which in turn reacts with the aniline or phenylenediamine to form a Schiff base and is thus consumed. The Schiff base forms the intended product by means of a dehydrogenation reaction, and the hydrogen evolved at this time reduces the phenol to form a cyclohexanone. The phenol present in excess thus becomes in the system a solvent, a starting material for the cyclohexanone, and an acceptor of the hydrogen that forms as a by-product at the time of formation of the intended product. Hence, it becomes possible to obtain the intended product at a high selectivity from the anilines and phenylenediamines. The process of this invention is an advantageous process for the industrial production of especially the nuclearly substituted diphenylamines.

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