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Catalog Number:
46023
CAS Number:
367-31-7
4-Fluoro-1,2-phénylènediamine
Purity:
≥ 98% (CG)
Synonym(s):
1,2-Diamino-4-fluorobenzène
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Product Information

4-Fluoro-1,2-phenylenediamine is a versatile chemical compound widely recognized for its applications in the dye and pigment industries. This aromatic amine features a fluorine substituent, which enhances its reactivity and stability, making it an ideal candidate for synthesizing various azo dyes and pigments. Its unique structure allows for improved colorfastness and brightness in textile applications, providing manufacturers with a competitive edge in producing high-quality, vibrant products.

In addition to its use in dyes, 4-Fluoro-1,2-phenylenediamine is also valuable in the field of pharmaceuticals and agrochemicals. It serves as an intermediate in the synthesis of biologically active compounds, contributing to the development of new drugs and crop protection agents. Researchers appreciate its ability to facilitate complex chemical reactions, leading to innovative solutions in medicinal chemistry and agricultural science. With its broad range of applications and benefits, 4-Fluoro-1,2-phenylenediamine stands out as a crucial compound for professionals seeking reliable and effective materials for their projects.

Synonyms
1,2-Diamino-4-fluorobenzène
CAS Number
367-31-7
Purity
≥ 98% (CG)
Molecular Formula
C6H7FN2
Molecular Weight
126.13
MDL Number
MFCD00042228
PubChem ID
164584
Melting Point
92 - 96 °C
Appearance
Poudre rouge à bleu foncé à noire à cristal
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
1,2-Diamino-4-fluorobenzène
CAS Number
367-31-7
Purity
≥ 98% (CG)
Molecular Formula
C6H7FN2
Molecular Weight
126.13
MDL Number
MFCD00042228
PubChem ID
164584
Melting Point
92 - 96 °C
Appearance
Poudre rouge à bleu foncé à noire à cristal
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Fluoro-1,2-phenylenediamine is widely utilized in research focused on:

  • Dye Manufacturing: This compound serves as a key intermediate in the synthesis of azo dyes, which are extensively used in textiles and printing. Its unique properties enhance colorfastness and vibrancy.
  • Pharmaceutical Development: It plays a significant role in the development of pharmaceuticals, particularly in the synthesis of compounds that exhibit anti-cancer and anti-inflammatory properties, making it valuable in medicinal chemistry.
  • Polymer Chemistry: The compound is used to create specialty polymers and resins, which are essential in producing durable materials for various applications, including coatings and adhesives.
  • Analytical Chemistry: It is employed as a reagent in various analytical techniques, such as chromatography, aiding in the detection and quantification of other chemical substances.
  • Research in Material Science: The unique electronic properties of this compound make it a candidate for research in organic electronics, including applications in organic light-emitting diodes (OLEDs) and solar cells.

Citations