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4-Bromo-2-chloro-5-(trifluoromethoxy)aniline is a chemical compound characterized by the presence of bromine, chlorine, and trifluoromethoxy groups attached to an aniline base. The halogens, bromine and chlorine, enhance the reactivity of the molecule, while the trifluoromethoxy group contributes to its overall stability. 4-broMo-2-chloro-5-(trifluoroMethoxy)aniline is versatile in various chemical reactions, particularly in organic synthesis, due to its functional groups. However, it must be handled with caution due to its potential toxicity.

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  • 115844-00-3 Structure
  • Basic information

    1. Product Name: 4-broMo-2-chloro-5-(trifluoroMethoxy)aniline
    2. Synonyms: 4-broMo-2-chloro-5-(trifluoroMethoxy)aniline;4-bromo-2-chloro-5-(trifluoromethoxy)benzenamine
    3. CAS NO:115844-00-3
    4. Molecular Formula: C7H4BrClF3NO
    5. Molecular Weight: 290.4649696
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115844-00-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 245.7±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.812±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 0.71±0.10(Predicted)
    10. CAS DataBase Reference: 4-broMo-2-chloro-5-(trifluoroMethoxy)aniline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-broMo-2-chloro-5-(trifluoroMethoxy)aniline(115844-00-3)
    12. EPA Substance Registry System: 4-broMo-2-chloro-5-(trifluoroMethoxy)aniline(115844-00-3)
  • 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: 115844-00-3(Hazardous Substances Data)

115844-00-3 Usage

Uses

Used in Organic Synthesis:
4-Bromo-2-chloro-5-(trifluoromethoxy)aniline is used as a building block in organic synthesis for its unique combination of functional groups, which can be utilized in the creation of a wide range of chemical products.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 4-bromo-2-chloro-5-(trifluoromethoxy)aniline is used as a precursor in the development of new drugs, leveraging its reactive and stable characteristics to form novel medicinal compounds.
Used in Material Sciences:
4-Bromo-2-chloro-5-(trifluoromethoxy)aniline is employed in material sciences for its potential to contribute to the development of new materials with specific properties, such as enhanced stability or reactivity, depending on the application requirements.
The specific uses of 4-bromo-2-chloro-5-(trifluoromethoxy)aniline can vary greatly depending on the field of study or industry, highlighting its adaptability and importance in chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 115844-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,4 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115844-00:
(8*1)+(7*1)+(6*5)+(5*8)+(4*4)+(3*4)+(2*0)+(1*0)=113
113 % 10 = 3
So 115844-00-3 is a valid CAS Registry Number.

115844-00-3SDS

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 4-bromo-2-chloro-5-(trifluoromethoxy)aniline

1.2 Other means of identification

Product number -
Other names Benzenamine, 4-bromo-2-chloro-5-(trifluoromethoxy)-

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:115844-00-3 SDS

115844-00-3Relevant articles and documents

NOVEL INHIBITORS OF HEPATITIS C VIRUS

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Paragraph 0241, (2015/09/22)

The invention provides compounds of formula (I): wherein the variables are defined in the specification, or a pharmaceutically-acceptable salt thereof, that are inhibitors of replication of the hepatitis C virus. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat hepatitis C viral infections, and processes and intermediates useful for preparing such compounds.

HEPATITIS C VIRUS INHIBITORS

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Paragraph 0291, (2013/05/21)

The invention provides compounds of formula (I): wherein the variables are defined in the specification, or a pharmaceutically-acceptable salt thereof, that are inhibitors of replication of the hepatitis C virus. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat hepatitis C viral infections, and processes and intermediates useful for preparing such compounds.

HEPATITIS C VIRUS INHIBITORS

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Paragraph 0260; 0261, (2013/11/06)

The invention provides compounds of formulas (I) or (II): wherein the variables are defined in the specification, or a pharmaceutically-acceptable salt thereof, that are inhibitors of replication of the hepatitis C virus. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat hepatitis C viral infections, and processes and intermediates useful for preparing such compounds.

PIPERAZINE-PIPERIDINE COMPOUNDS AS HEPATITIS C VIRUS INHIBITORS

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Paragraph 0277; 0278, (2013/11/06)

The invention provides compounds of formula (I): wherein the variables are defined in the specification, or a pharmaceutically-acceptable salt thereof, that are inhibitors of replication of the hepatitis C virus. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat hepatitis C viral infections, and processes and intermediates useful for preparing such compounds.

NOVEL INHIBITORS OF HEPATITIS C VIRUS

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, (2012/05/20)

The invention provides compounds of formula (I): wherein the variables are defined in the specification, or a pharmaceutically-acceptable salt thereof, that are inhibitors of replication of the hepatitis C virus. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat hepatitis C viral infections, and processes and intermediates useful for preparing such compounds.

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