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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-ethyl-1-benzofuran-3-carbaldehyde

CCc1oc2c(c1C=O)cccc2 Request for Quotation
Chemical Name: 2-ethyl-1-benzofuran-3-carbaldehyde
CAS Number: 10035-41-3
Product Number: AG0001PJ(AGN-PC-0KPYS2)
Synonyms:
MDL No:
Molecular Formula: C11H10O2
Molecular Weight: 174.1959

Identification/Properties

Computed Properties
Molecular Weight:
174.199g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
174.068g/mol
Monoisotopic Mass:
174.068g/mol
Topological Polar Surface Area:
30.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
191
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Ethylbenzofuran-3-carbaldehyde is a versatile compound frequently utilized in chemical synthesis as a valuable building block. Its unique structure provides opportunities for various functionalization reactions, making it an essential intermediate in the preparation of diverse organic compounds.In organic synthesis, 2-Ethylbenzofuran-3-carbaldehyde is often employed as a key starting material for the synthesis of pharmaceutically relevant molecules, agrochemicals, fragrances, and other fine chemicals. Its aldehyde group serves as a reactive site for the introduction of different functional groups, allowing chemists to create complex molecular structures efficiently.Furthermore, the presence of the benzofuran ring in the molecule imparts specific properties that can be advantageous in drug discovery and material science. The benzofuran moiety is known for its bioactive properties, and incorporating it into molecules can potentially enhance their biological activity.Overall, the application of 2-Ethylbenzofuran-3-carbaldehyde in chemical synthesis underscores its importance as a key reagent for constructing intricate organic molecules with diverse functionalities and applications.