Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
44946
CAS Number:
19654-19-4
2-(4-Bromophenyl)benzothiazole
Purity:
≥ 98% (GC)
Synonym(s):
1-(2-Benzothiazolyl)-4-bromobenzene
Documents
$138.31 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

2-(4-Bromophenyl)benzothiazole is a versatile compound known for its unique properties and applications in various fields, particularly in organic synthesis and materials science. This compound features a bromophenyl group that enhances its reactivity, making it an excellent candidate for use in the development of pharmaceuticals, agrochemicals, and advanced materials. Its structure allows for effective interactions in biological systems, which can be leveraged in drug discovery and development processes. Researchers have utilized 2-(4-Bromophenyl)benzothiazole in the synthesis of novel compounds that exhibit significant biological activity, including antimicrobial and anticancer properties.

Additionally, this compound serves as a valuable intermediate in the production of dyes and pigments, contributing to the color stability and performance of end products. Its ability to form stable complexes with metals further expands its utility in catalysis and sensor applications. With its broad range of applications and benefits, 2-(4-Bromophenyl)benzothiazole stands out as a crucial component for professionals seeking innovative solutions in their respective fields.

Synonyms
1-(2-Benzothiazolyl)-4-bromobenzene
CAS Number
19654-19-4
Purity
≥ 98% (GC)
Molecular Formula
C13H8BrNS
Molecular Weight
290.18
MDL Number
MFCD00579199
PubChem ID
2320602
Melting Point
132 - 135 °C
Appearance
White to light yellow to green powder to crystal
Conditions
Store at 2 - 8 °C
General Information
Synonyms
1-(2-Benzothiazolyl)-4-bromobenzene
CAS Number
19654-19-4
Purity
≥ 98% (GC)
Molecular Formula
C13H8BrNS
Molecular Weight
290.18
MDL Number
MFCD00579199
PubChem ID
2320602
Melting Point
132 - 135 °C
Appearance
White to light yellow to green powder to crystal
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(4-Bromophenyl)benzothiazole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents. Its unique structure allows for modifications that enhance biological activity.
  • Material Science: It is used in the formulation of advanced materials, including polymers and coatings, where its properties contribute to improved thermal stability and chemical resistance.
  • Fluorescent Probes: The compound is employed in creating fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes with high specificity and sensitivity.
  • Agricultural Chemicals: It finds applications in the development of agrochemicals, particularly fungicides, due to its effectiveness in inhibiting fungal growth, thus supporting crop protection efforts.
  • Analytical Chemistry: This chemical is used as a reagent in various analytical methods, including spectrophotometry, to detect and quantify other compounds, enhancing the accuracy of chemical analyses.

Citations