Benzofuran, 4-ethenyl-2,3-dihydro-


Chemical Name: Benzofuran, 4-ethenyl-2,3-dihydro-
CAS Number: 230642-84-9
Product Number: AG002M2W(AGN-PC-009A0I)
Synonyms:
MDL No:
Molecular Formula: C10H10O
Molecular Weight: 146.1858

Identification/Properties


Computed Properties
Molecular Weight:
146.189g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
146.073g/mol
Monoisotopic Mass:
146.073g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



4-Vinyl-2,3-dihydrobenzofuran, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its primary application lies in organic chemistry as a key building block for the synthesis of various complex molecules and functional materials. This compound serves as a valuable intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural features and reactivity.In chemical synthesis, 4-Vinyl-2,3-dihydrobenzofuran acts as a crucial starting material for the construction of heterocyclic compounds through diverse synthetic pathways. Its vinyl group enables it to participate in a range of important reactions, such as palladium-catalyzed cross-coupling reactions, cycloadditions, and aromatic transformations. These chemical transformations allow for the introduction of different functional groups and modifications, leading to the generation of structurally diverse and biologically active compounds.Furthermore, the presence of the dihydrobenzofuran moiety in 4-Vinyl-2,3-dihydrobenzofuran imparts specific physicochemical properties to the synthesized molecules, making them suitable for applications in medicinal chemistry, material science, and catalysis. By incorporating this compound into the molecular design, researchers can access novel compounds with potential applications in drug discovery, materials development, and chemical processes.Overall, the strategic use of 4-Vinyl-2,3-dihydrobenzofuran in chemical synthesis offers a wide range of possibilities for creating valuable compounds with diverse functionalities and applications. Its versatility and synthetic utility make it an indispensable tool for researchers and chemists working on the development of new molecules with targeted properties.