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1,2-Dichloro-3,4,5,6-tetrafluorobenzene is an organic compound with the chemical formula C6Cl2F4. It is a halogenated aromatic compound, characterized by the presence of two chlorine atoms and four fluorine atoms attached to a benzene ring. This molecule exhibits unique chemical and physical properties due to the electron-withdrawing nature of fluorine and the electron-donating nature of chlorine, which can influence its reactivity and stability. It is a colorless liquid with a high boiling point and is used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is also known for its potential applications in materials science, such as in the development of new polymers and coatings. Due to its halogenated nature, 1,2-dichlorotetrafluorobenzene requires careful handling and is subject to regulations regarding its production, use, and disposal to minimize environmental and health risks.

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  • 1198-59-0 Structure
  • Basic information

    1. Product Name: 1,2-Dichloro-3,4,5,6-tetrafluorobenzene
    2. Synonyms: 1,2-Dichloro-3,4,5,6-tetrafluorobenzene
    3. CAS NO:1198-59-0
    4. Molecular Formula: C6Cl2F4
    5. Molecular Weight: 218.96
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1198-59-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 157.7°C (rough estimate)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.6252 (estimate)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2-Dichloro-3,4,5,6-tetrafluorobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Dichloro-3,4,5,6-tetrafluorobenzene(1198-59-0)
    11. EPA Substance Registry System: 1,2-Dichloro-3,4,5,6-tetrafluorobenzene(1198-59-0)
  • 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: 1198-59-0(Hazardous Substances Data)

1198-59-0 Usage

Physical state

Colorless liquid

Uses

Intermediate in the production of pharmaceuticals, pesticides, and other organic compounds

Classification

Halogenated organic compound (contains chlorine and fluorine atoms)

Stability

High stability

Reactivity

Low reactivity

Importance

Valuable building block for the synthesis of complex organic molecules

Safety

Toxic, requires proper handling and management to prevent harm

Check Digit Verification of cas no

The CAS Registry Mumber 1198-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1198-59:
(6*1)+(5*1)+(4*9)+(3*8)+(2*5)+(1*9)=90
90 % 10 = 0
So 1198-59-0 is a valid CAS Registry Number.

1198-59-0SDS

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 1,2-dichloro-3,4,5,6-tetrafluorobenzene

1.2 Other means of identification

Product number -
Other names 1,2,3,4-Tetrafluor-5,6-dichlor-benzol

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:1198-59-0 SDS

1198-59-0Relevant articles and documents

Synergism in catalytic halogen-exchange fluorination of 4-chloronitro- and dichlorotetrafluorobenzenes

Shipilov,Bykova,Elokhova,Igumnov

, p. 487 - 491 (2003)

Synergism was studied in catalytic halogen-exchange fluorination of 4-chloronitro- and dichlorotetrafluorobenzenes. The synergistic effect in the fluorination of chloroaromatic compounds with potassium fluoride was mainly attributed to separation of the activation functions of catalysts with respect to substrate molecules.

Catalytic and noncatalytic ammonolysis of polyfluorinated 1,3-dichlorobenzenes

Selivanova,Pokrovskii,Shteingarts

, p. 1023 - 1029 (2007/10/03)

Reactions of 1,3-dichlorotetrafluorobenzene and 1,3-dichloro-2,4,6-trifluorobenzene with aqueous ammonia in the presence and in the absence of copper(I) salt lead to fluorine replacement by amino group in the para and ortho positions with respect to the chlorine atom. Ammonolysis of the resulting chloropolyfluoroanilines in the absence of a catalyst involves replacement of fluorine atom in the meta position with respect to the amino group. In the presence of copper(I) salt, catalytic aminodechlorination occurs at the para and ortho positions with respect to the amino group introduced in the first stage.

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