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Catalog Number:
36165
CAS Number:
887144-97-0
3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole
Purity:
≥ 98% (NMR)
Hazmat
Documents
$64.90 /100MG
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Product Information

3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole is a versatile compound known for its unique chemical structure and properties, making it valuable in various applications. This compound features a trifluoromethyl group, which enhances its reactivity and stability, making it an excellent candidate for use in organic synthesis and pharmaceutical development. Researchers have utilized this compound in the synthesis of complex organic molecules, particularly in the development of fluorinated pharmaceuticals, where the trifluoromethyl group can significantly influence biological activity and pharmacokinetics.

Additionally, 3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole serves as a useful reagent in the field of materials science, where it can be employed in the creation of advanced materials with tailored properties. Its unique characteristics allow for the modification of polymeric materials, enhancing their performance in various industrial applications. With its growing relevance in both academic research and industrial applications, this compound stands out as a key player in the development of innovative chemical solutions.

CAS Number
887144-97-0
Purity
≥ 98% (NMR)
Molecular Formula
C10H10F3IO
Molecular Weight
330.09
MDL Number
MFCD10567056
PubChem ID
16043572
Melting Point
75 - 79 ?C
Appearance
White solid
Conditions
Store at 2 - 8 °C
General Information
CAS Number
887144-97-0
Purity
≥ 98% (NMR)
Molecular Formula
C10H10F3IO
Molecular Weight
330.09
MDL Number
MFCD10567056
PubChem ID
16043572
Melting Point
75 - 79 ?C
Appearance
White solid
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a valuable reagent in organic chemistry, particularly for the synthesis of complex molecules. Its unique structure allows for selective reactions, making it a preferred choice for chemists aiming to create specific compounds efficiently.
  • Fluorination Reactions: Its trifluoromethyl group enhances its utility in fluorination processes, which are essential in pharmaceuticals and agrochemicals. This application is crucial for developing compounds with improved biological activity and stability.
  • Material Science: The compound is employed in the development of advanced materials, such as polymers and coatings. Its properties contribute to enhanced durability and resistance to environmental factors, making it suitable for industrial applications.
  • Medicinal Chemistry: Researchers utilize this chemical in the design of new drugs, particularly those targeting specific diseases. Its ability to modify biological activity provides a pathway for creating more effective therapeutic agents.
  • Analytical Chemistry: It is also used as a standard in analytical methods, aiding in the detection and quantification of various substances. This application is vital for quality control in pharmaceutical and chemical industries.

Citations