2-Amino-3-chlorobenzotrifluoride

≥97.0%

  • Product Code: 59139
  Alias:    2-Chloro-6-trifluoromethylaniline
  CAS:    433-94-3
Molecular Weight: 195.57 g./mol Molecular Formula: C₇H₅ClF₃N
EC Number: 207-091-8 MDL Number: MFCD00272565
Melting Point: Boiling Point:
Density: 1.42 Storage Condition: room temperature
Product Description: 2-Amino-3-chlorobenzotrifluoride is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure, featuring both amino and trifluoromethyl groups, makes it valuable in the development of compounds with specific biological activities. In the pharmaceutical industry, it is often utilized to create active ingredients for drugs targeting neurological disorders, inflammation, and infections. Additionally, its role in agrochemicals includes the production of herbicides and pesticides, where the trifluoromethyl group enhances the efficacy and stability of the final product. The compound’s reactivity also allows for further functionalization, enabling the creation of diverse derivatives for specialized applications in material science and organic synthesis.
Product Specification:
Test Specification
PurityGC 97-100
REFRACTIVE INDEX N20D 1.496-1.499
SPECIFIC GRAVITY 2020C 1.422-1.427
APPEARANCE COLORLESS TO PALE YELLOW LIQUID
INFRARED SPECTROMETRY Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days €9.76
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5.000 10-20 days €22.16
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25.000 10-20 days €70.76
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100.000 10-20 days €208.95
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2-Amino-3-chlorobenzotrifluoride
2-Amino-3-chlorobenzotrifluoride is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure, featuring both amino and trifluoromethyl groups, makes it valuable in the development of compounds with specific biological activities. In the pharmaceutical industry, it is often utilized to create active ingredients for drugs targeting neurological disorders, inflammation, and infections. Additionally, its role in agrochemicals includes the production of herbicides and pesticides, where the trifluoromethyl group enhances the efficacy and stability of the final product. The compound’s reactivity also allows for further functionalization, enabling the creation of diverse derivatives for specialized applications in material science and organic synthesis.
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