2-chloro-1-(5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)indolin-1-yl)ethanone

98%

  • Product Code: 67417
  CAS:    1704067-44-6
Molecular Weight: 321.61 g./mol Molecular Formula: C₁₆H₂₁BClNO₃
EC Number: MDL Number: MFCD28384363
Melting Point: Boiling Point:
Density: Storage Condition:  2-8°C
Product Description: This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a dioxaborolane group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. This reaction is crucial in constructing complex molecules, including drug candidates and biologically active compounds. Additionally, the indoline moiety in its structure suggests potential applications in the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases. Its versatility in chemical transformations makes it a key component in medicinal chemistry research and industrial-scale production of fine chemicals.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days Ft540,860.22
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2-chloro-1-(5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)indolin-1-yl)ethanone
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a dioxaborolane group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. This reaction is crucial in constructing complex molecules, including drug candidates and biologically active compounds. Additionally, the indoline moiety in its structure suggests potential applications in the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases. Its versatility in chemical transformations makes it a key component in medicinal chemistry research and industrial-scale production of fine chemicals.
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