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1,2,4-Trichloro-5-fluorobenzene is a chemical compound belonging to the class of fluorobenzenes, characterized by the molecular formula C6H2Cl3F. It features a benzene ring with three chlorine atoms and one fluorine atom attached, making it a versatile intermediate in the synthesis of various organic compounds.

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  • 400-04-4 Structure
  • Basic information

    1. Product Name: 1,2,4-trichloro-5-fluorobenzene
    2. Synonyms: 1,2,4-trichloro-5-fluorobenzene
    3. CAS NO:400-04-4
    4. Molecular Formula: C6H2Cl3F
    5. Molecular Weight: 199.4374832
    6. EINECS: 206-921-6
    7. Product Categories: N/A
    8. Mol File: 400-04-4.mol
  • Chemical Properties

    1. Melting Point: 62 °C
    2. Boiling Point: 211.1°Cat760mmHg
    3. Flash Point: 86°C
    4. Appearance: /
    5. Density: 1.54g/cm3
    6. Vapor Pressure: 0.27mmHg at 25°C
    7. Refractive Index: 1.544
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,2,4-trichloro-5-fluorobenzene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2,4-trichloro-5-fluorobenzene(400-04-4)
    12. EPA Substance Registry System: 1,2,4-trichloro-5-fluorobenzene(400-04-4)
  • 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: 400-04-4(Hazardous Substances Data)

400-04-4 Usage

Uses

Used in Pharmaceutical Industry:
1,2,4-Trichloro-5-fluorobenzene is used as a key intermediate in the synthesis of pharmaceuticals for its chemical properties and reactivity, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
1,2,4-trichloro-5-fluorobenzene serves as an essential building block in the production of agrochemicals, aiding in the creation of effective pesticides and other agricultural chemicals to protect crops and enhance yields.
Used in Organic Synthesis:
1,2,4-Trichloro-5-fluorobenzene is utilized as a versatile intermediate in organic synthesis, enabling the production of a wide range of organic compounds for various applications, including specialty chemicals and materials.
It is crucial to handle 1,2,4-trichloro-5-fluorobenzene with care and adhere to proper safety protocols due to its potential hazards and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 400-04-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 400-04:
(5*4)+(4*0)+(3*0)+(2*0)+(1*4)=24
24 % 10 = 4
So 400-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl3F/c7-3-1-5(9)6(10)2-4(3)8/h1-2H

400-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4-trichloro-5-fluorobenzene

1.2 Other means of identification

Product number -
Other names Benzene,1,2,4-trichloro-5-fluoro

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:400-04-4 SDS

400-04-4Relevant articles and documents

Preparation process of fluorine substituted aromatic compound

-

, (2008/06/13)

A preparation process of a fluorine substituted aromatic compound comprising reacting an alkali metal or alkali earth metal salt of an aromatic compound having a hydroxy group with an organic fluorinating agent is disclosed. As a representative fluorinating agent, a bis-dialkylamino-difluoromethane compound, for example, 2,2′-difluoro-1,3-dimethylimidazolidine, is exemplified. According to the process, an industrially useful fluorinated aromatic compound, for example, a fluorobenzene, a fluorine substituted benzophenone, a fluorine substituted diarylsulfone can be prepared with ease in economy without specific equipment.

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