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2-amino-3,4,5,6-tetrachlorobenzoic acid is a chemical compound with the molecular formula C7H3Cl4NO2. It is a derivative of benzoic acid, featuring an amino group attached to the third carbon atom and four chlorine atoms on the benzene ring. 2-amino-3,4,5,6-tetrachlorobenzoic acid is known for its potential applications in various industries due to its unique chemical structure.

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  • 6923-69-9 Structure
  • Basic information

    1. Product Name: 2-amino-3,4,5,6-tetrachlorobenzoic acid
    2. Synonyms: 2-amino-3,4,5,6-tetrachlorobenzoic acid
    3. CAS NO:6923-69-9
    4. Molecular Formula: C7H3Cl4NO2
    5. Molecular Weight: 274.92
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6923-69-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 404.6 °C at 760 mmHg
    3. Flash Point: 198.5 °C
    4. Appearance: /
    5. Density: 1.808 g/cm3
    6. Vapor Pressure: 2.84E-07mmHg at 25°C
    7. Refractive Index: 1.673
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-amino-3,4,5,6-tetrachlorobenzoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-amino-3,4,5,6-tetrachlorobenzoic acid(6923-69-9)
    12. EPA Substance Registry System: 2-amino-3,4,5,6-tetrachlorobenzoic acid(6923-69-9)
  • 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: 6923-69-9(Hazardous Substances Data)

6923-69-9 Usage

Uses

Used in Pharmaceutical Industry:
2-amino-3,4,5,6-tetrachlorobenzoic acid is used as an intermediate in the production of various pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of drugs with specific therapeutic properties.
Used in Dye Industry:
In the dye industry, 2-amino-3,4,5,6-tetrachlorobenzoic acid is utilized as an intermediate for the synthesis of dyes with particular color characteristics. Its chlorine and amino groups contribute to the dye's stability and color intensity.
Used in Agrochemical Industry:
2-amino-3,4,5,6-tetrachlorobenzoic acid serves as an intermediate in the development of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the creation of effective compounds for agricultural applications.
Used as a Research Reagent:
In the field of organic synthesis, 2-amino-3,4,5,6-tetrachlorobenzoic acid is employed as a research reagent. It aids scientists in understanding the structure-activity relationship of certain compounds, contributing to the advancement of chemical knowledge.
Safety Precautions:
Due to its toxic and harmful nature, appropriate safety measures should be taken when handling 2-amino-3,4,5,6-tetrachlorobenzoic acid. It is crucial to avoid ingestion, inhalation, or skin contact to minimize health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 6923-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6923-69:
(6*6)+(5*9)+(4*2)+(3*3)+(2*6)+(1*9)=119
119 % 10 = 9
So 6923-69-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl4NO2/c8-2-1(7(13)14)6(12)5(11)4(10)3(2)9/h12H2,(H,13,14)

6923-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-3,4,5,6-tetrachlorobenzoic acid

1.2 Other means of identification

Product number -
Other names tetrachloroanthranilic acid

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:6923-69-9 SDS

6923-69-9Relevant articles and documents

Novel functionalized indigo derivatives for organic electronics

Klimovich, Irina V.,Zhilenkov, Alexander V.,Кuznetsova, Lidiya I.,Frolova, Lubov A.,Yamilova, Olga R.,Troyanov, Sergey I.,Lyssenko, Konstantin A.,Troshin, Pavel A.

, (2020/11/24)

A series of nine novel indigo derivatives, including diiodoindigo, octahalogenated indigoids and compounds with extended π-conjugated system, were synthesized, characterized and investigated as semiconductor materials in organic field-effect transistors (OFETs). Among them, 6,6′-diiodoindigo demonstrated the ambipolar behavior with balanced p-type and n-type mobilities. The complete substitution of hydrogens at the indigo core with halogen atoms led to low electron mobilities in OFETs. An extension of the conjugated system through the introduction of small aromatic substituents (thiophene and phenyl) resulted in predominant p-type behavior. Fusion of aromatic rings resulted in z-shaped dibenzoindigo, which showed poor charge transport properties due to the non-optimal arrangement of molecules along each other in the crystal lattice. The acquired data fulfilled the previously reported model based on the relationship between the chemical nature of substituents and their positions at the indigo core, optoelectronic properties of materials and their performance in OFETs. The results of this study will be useful for rational design of a new generation of the indigo-based semiconductors for biocompatible organic electronics.

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