4-Bromo-2,5-dimethyl-2H-1,2,3-triazole

97%

  • Product Code: 119250
  CAS:    942060-54-0
Molecular Weight: 176.01 g./mol Molecular Formula: C₄H₆BrN₃
EC Number: MDL Number: MFCD14706834
Melting Point: Boiling Point: 244°C at 760 mmHg
Density: Storage Condition: 2-8°C, store under inert gas
Product Description: This chemical is primarily used in the field of organic synthesis as a versatile building block for the development of more complex molecules. It serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for the introduction of functional groups, enabling the creation of compounds with specific biological or chemical properties. Additionally, it is employed in research and development for the synthesis of novel triazole derivatives, which are often explored for their potential therapeutic applications, including antimicrobial, antifungal, and anticancer activities. Its role in click chemistry reactions further enhances its utility in creating diverse molecular architectures for industrial and academic purposes.
Product Specification:
Test Specification
Appearance Colorless To Pale-yellow To Yellow-brown Liquid
Purity (%) 96.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $156.02
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0.250 10-20 days $254.73
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1.000 10-20 days $794.18
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4-Bromo-2,5-dimethyl-2H-1,2,3-triazole
This chemical is primarily used in the field of organic synthesis as a versatile building block for the development of more complex molecules. It serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for the introduction of functional groups, enabling the creation of compounds with specific biological or chemical properties. Additionally, it is employed in research and development for the synthesis of novel triazole derivatives, which are often explored for their potential therapeutic applications, including antimicrobial, antifungal, and anticancer activities. Its role in click chemistry reactions further enhances its utility in creating diverse molecular architectures for industrial and academic purposes.
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