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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)-

7-Benzofurancarboxaldehyde

O=Cc1cccc2c1occ2 Request for Quotation
Chemical Name: 7-Benzofurancarboxaldehyde
CAS Number: 95333-14-5
Product Number: AG003O27(AGN-PC-0NGBH2)
Synonyms:
MDL No: MFCD08272125
Molecular Formula: C9H6O2
Molecular Weight: 146.1427

Identification/Properties

Properties
BP:
251.549°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
146.145g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
146.037g/mol
Monoisotopic Mass:
146.037g/mol
Topological Polar Surface Area:
30.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
156
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-H312-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzofuran-7-carbaldehyde is a versatile compound that plays a crucial role in chemical synthesis. As a key precursor in organic reactions, this aldehyde serves as a building block for the synthesis of various valuable molecules and pharmaceuticals. Its unique structure and reactivity make it particularly useful in the creation of complex heterocyclic compounds, which are essential in drug development and material science.One of the main applications of benzofuran-7-carbaldehyde is in the construction of biologically active molecules such as anticancer agents, antimicrobial compounds, and antioxidants. By undergoing diverse chemical transformations, this compound can be modified to introduce specific functional groups or stereochemistry, allowing for the fine-tuning of biological activity and pharmacokinetic properties.Furthermore, benzofuran-7-carbaldehyde is employed in the synthesis of natural products and dyes due to its ability to participate in various carbon-carbon and carbon-heteroatom bond-forming reactions. Its presence in the molecular structure imparts desirable characteristics and properties to the final products, making it a valuable tool for organic chemists and researchers in the field of medicinal chemistry and material science.Overall, the versatile nature of benzofuran-7-carbaldehyde makes it an indispensable compound in the realm of chemical synthesis, offering endless opportunities for the creation of novel molecules with diverse applications.