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4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98 is an aromatic amine organic compound characterized by a phenylenediamine moiety with bromine and fluorine substituents. It is known for its ability to form reactive intermediates that bind effectively to hair proteins, making it a key component in the formulation of hair dyes and pigments.

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  • 153505-37-4 Structure
  • Basic information

    1. Product Name: 4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98
    2. Synonyms: 4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98;4-Bromo-5-fluoro-1,2-phenylenediamine 98%;4-Bromo-5-fluorobenzene-1,2-diamine 97%;4-Bromo-5-fluorophenylene-1,2-diamine, 4-Bromo-1,2-diamino-5-fluorobenzene;1,2-BenzenediaMine, 4-broMo-5-fluoro-;4-Bromo-5-fluorophenylene-1,2-diamine, 1-Bromo-4,5-diamino-2-fluorobenzene;4-Bromo-5-fluorobenzene-1,2-diamine97%
    3. CAS NO:153505-37-4
    4. Molecular Formula: C6H6BrFN2
    5. Molecular Weight: 205.0294
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153505-37-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 297 °C at 760 mmHg
    3. Flash Point: 133.4 °C
    4. Appearance: /
    5. Density: 1.792 g/cm3
    6. Vapor Pressure: 0.00139mmHg at 25°C
    7. Refractive Index: 1.663
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: N/A
    10. PKA: 3.15±0.10(Predicted)
    11. CAS DataBase Reference: 4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98(153505-37-4)
    13. EPA Substance Registry System: 4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98(153505-37-4)
  • Safety Data

    1. Hazard Codes: Xi
    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: 153505-37-4(Hazardous Substances Data)

153505-37-4 Usage

Uses

Used in Hair Dye Industry:
4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98 is used as a colorant for hair dyes due to its capacity to create long-lasting color by binding to hair proteins. Its presence in hair dye formulations contributes to the development of a wide range of shades and tones.
Used in Pigment Industry:
In the pigment industry, 4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98 is utilized as a pigment precursor, enabling the production of stable and vibrant pigments for various applications, including cosmetics and other industrial uses.
Safety Considerations:
It is crucial to handle 4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98 with care due to its potential hazards. Proper storage and handling in accordance with safety guidelines are essential to prevent any adverse effects during its use in manufacturing processes.

Check Digit Verification of cas no

The CAS Registry Mumber 153505-37-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,5,0 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 153505-37:
(8*1)+(7*5)+(6*3)+(5*5)+(4*0)+(3*5)+(2*3)+(1*7)=114
114 % 10 = 4
So 153505-37-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BrFN2/c7-3-1-5(9)6(10)2-4(3)8/h1-2H,9-10H2

153505-37-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-5-fluorobenzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names 4-bromo-5-fluoro-benzene-1,2-diamine

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:153505-37-4 SDS

153505-37-4Relevant articles and documents

AMINO-QUINOLINES AS KINASE INHIBITORS

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, (2015/09/23)

Disclosed are quinoline compounds having the formula: wherein R1, R2 and A are as defined herein, and methods of making and using the same.

SERINE/THREONINE PAK1 INHIBITORS

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, (2013/03/26)

Compounds having the formula I wherein A, Z, R1a, R1b, R2, R3, R4, R5, R6, R7, R9, R10, Ra, Rb and n are as defined herein are inhibitors of PAK1. Also disclosed are compositions and methods for treating cancer and hyperproliferative disorders.

ANTI-VIRAL COMPOUNDS

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, (2012/06/30)

Compounds effective in inhibiting replication of Hepatitis C virus ("HCV") are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.

NOVEL COMPOUNDS AS ANTAGONISTS OR INVERSE AGONISTS FOR OPIOID RECEPTORS

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Page/Page column 69, (2010/09/07)

This invention relates to novel compounds which are antagonists or inverse agonists at one or more of the opioid receptors, to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy.

Benzimidazole Modulators of VR1

-

Page/Page column 175, (2008/06/13)

The invention is directed to compounds of Formula (I): to pharmaceutical compositions containing such compounds and to methods of treatment using them.

Glycine receptor antagonists and the use thereof

-

, (2008/06/13)

Methods of treating or preventing neuronal loss associated with stroke, ischemia, CNS trauma, hypoglycemia and surgery, as well as treating neurodegenerative diseases including Alzheimer's disease, amyotrophic lateral sclerosis, Huntington's disease and Down's syndrome, treating or preventing the adverse consequences of the hyperactivity of the excitatory amino acids, as well as treating anxiety, chronic pain, convulsions, inducing anesthesia and treating psychosis are disclosed by administering to an animal in need of such treatment a compound having high affinity for the glycine binding site, lacking PCP side effects and which crosses the blood brain barrier of the animal. Also disclosed are novel 1,4-dihydroquinoxaline-2,3-diones, and pharmaceutical compositions thereof. Also disclosed are highly soluble ammonium salts of 1,4-dihydroquinoxaline-2,3-diones.

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