4-iodo-2,3-dihydro-1H-indole


Chemical Name: 4-iodo-2,3-dihydro-1H-indole
CAS Number: 939759-03-2
Product Number: AG00H32Y(AGN-PC-00VAHX)
Synonyms:
MDL No:
Molecular Formula: C8H8IN
Molecular Weight: 245.0603

Identification/Properties


Computed Properties
Molecular Weight:
245.063g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
244.97g/mol
Monoisotopic Mass:
244.97g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
126
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



4-Iodoindoline is a versatile chemical compound that finds extensive use in synthetic chemistry due to its unique properties and reactivity. In chemical synthesis, 4-Iodoindoline serves as a valuable building block for the construction of various biologically active molecules, pharmaceuticals, and advanced materials. Its strategic placement of the iodine atom on the indoline ring provides a handle for further functionalization, making it a crucial intermediate in the synthesis of complex organic molecules. The inherent stability of the indoline ring system coupled with the electrophilic nature of the iodine substituent allows for efficient cross-coupling reactions, such as Suzuki-Miyaura, Heck, or Sonogashira couplings, leading to the creation of diverse molecular architectures.Moreover, the 4-Iodoindoline scaffold can undergo various transformations, including nucleophilic substitutions, metal-catalyzed reactions, and radical processes, enabling its incorporation into intricate molecular frameworks. The resulting products derived from 4-Iodoindoline synthesis exhibit a wide range of biological activities, making it a valuable tool in medicinal chemistry and drug discovery efforts.Overall, the application of 4-Iodoindoline in chemical synthesis exemplifies its significance as a key building block in the creation of novel molecules with promising properties and functionalities.