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Catalog Number:
41834
CAS Number:
5227-71-4
3,3-Dimethyl-2-methylene-1-phenylindoline
Grade:
suitable for Hematology & Histology
Synonym(s):
Phenyl Fischer Base
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Product Information

3,3-Dimethyl-2-methylene-1-phenylindoline is a versatile compound recognized for its unique structural features and potential applications in various fields. This indoline derivative exhibits remarkable stability and reactivity, making it an excellent candidate for use in organic synthesis and material science. Its distinctive properties allow it to function effectively as a building block in the development of advanced organic materials, including dyes and pigments, which are essential in the textile and coatings industries. Additionally, its photochemical characteristics make it suitable for applications in photonic devices and organic light-emitting diodes (OLEDs), where efficient light emission is crucial.

Researchers and industry professionals can leverage 3,3-Dimethyl-2-methylene-1-phenylindoline in the synthesis of novel compounds, enhancing the performance of electronic devices and improving colorfastness in textiles. Its ability to undergo various chemical transformations opens up avenues for innovation in drug discovery and development, particularly in creating compounds with enhanced biological activity. With its blend of stability and reactivity, this compound stands out as a valuable resource for those looking to push the boundaries of material science and organic chemistry.

Synonyms
Phenyl Fischer Base
CAS Number
5227-71-4
Grade
suitable for Hematology & Histology
Molecular Formula
C17H17N
Molecular Weight
235.32
MDL Number
MFCD00438714
PubChem ID
78895
Density
1.034 g/mL at 25 °C (Lit.)
Appearance
Colorless, orange or brown liquid
Boiling Point
169 - 170 °C (Lit.)
Refractive Index
n20D 1.61 (Lit.)
Conditions
Store at RT
General Information
Synonyms
Phenyl Fischer Base
CAS Number
5227-71-4
Grade
suitable for Hematology & Histology
Molecular Formula
C17H17N
Molecular Weight
235.32
MDL Number
MFCD00438714
PubChem ID
78895
Density
1.034 g/mL at 25 °C (Lit.)
Appearance
Colorless, orange or brown liquid
Boiling Point
169 - 170 °C (Lit.)
Refractive Index
n20D 1.61 (Lit.)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3,3-Dimethyl-2-methylene-1-phenylindoline is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as an important intermediate in the synthesis of various organic molecules, enabling chemists to create complex structures efficiently.
  • Fluorescent Dyes: It is used in the development of fluorescent dyes for biological imaging, providing researchers with tools to visualize cellular processes in real-time.
  • Photovoltaic Materials: The compound has applications in the formulation of organic photovoltaic devices, contributing to the advancement of renewable energy technologies.
  • Pharmaceutical Development: It plays a role in the synthesis of potential pharmaceutical agents, particularly in the search for new therapeutic compounds.
  • Material Science: This chemical is explored for its properties in creating novel materials, such as polymers with enhanced optical or electronic characteristics.

Citations