1H-Indole-2,3-dione, 5,6-difluoro-


Chemical Name: 1H-Indole-2,3-dione, 5,6-difluoro-
CAS Number: 774-47-0
Product Number: AG003467(AGN-PC-0KAD36)
Synonyms:
MDL No:
Molecular Formula: C8H3F2NO2
Molecular Weight: 183.1117

Identification/Properties


Properties
MP:
218-220℃
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
183.114g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
183.013g/mol
Monoisotopic Mass:
183.013g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
269
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



5,6-Difluoroindoline-2,3-dione is a versatile compound that finds wide application in chemical synthesis. This unique molecule serves as a crucial building block in the creation of various complex organic compounds due to its functional group reactivity and structural properties. One of the key applications of 5,6-Difluoroindoline-2,3-dione is its role as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 5,6-Difluoroindoline-2,3-dione acts as a pivotal starting material for the generation of diverse fused heterocyclic systems. Its fluorine substituents confer distinct reactivity patterns, enabling selective functionalization at specific positions within the molecule. This selectivity is particularly beneficial in intricate multi-step synthetic pathways where precise control over regiochemistry is essential for the successful formation of the desired product.Moreover, the presence of the indoline core in 5,6-Difluoroindoline-2,3-dione imparts additional structural diversity and complexity to the compounds synthesized from it. This structural motif is commonly found in biologically active molecules, making derivatives of 5,6-Difluoroindoline-2,3-dione valuable candidates for medicinal chemistry research and drug discovery efforts.Overall, the strategic incorporation of 5,6-Difluoroindoline-2,3-dione in chemical synthesis enables chemists to access a wide array of novel compounds with tailored properties and functionalities. Its versatile nature and synthetic utility make it a valuable tool for advancing the frontiers of organic chemistry and driving innovation in diverse fields of science and technology.