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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-Benzofurancarboxylic acid, 3-methyl-

OC(=O)c1oc2c(c1C)cccc2 Request for Quotation
Chemical Name: 2-Benzofurancarboxylic acid, 3-methyl-
CAS Number: 24673-56-1
Product Number: AG002P0L(AGN-PC-0JTL15)
Synonyms:
MDL No:
Molecular Formula: C10H8O3
Molecular Weight: 176.1687

Identification/Properties

Properties
MP:
194-197 °C
BP:
328.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
176.171g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
176.047g/mol
Monoisotopic Mass:
176.047g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
214
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
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Methylbenzofuran-2-carboxylic acid is a versatile compound that finds wide application in chemical synthesis. One key use of this compound is as a building block in the preparation of various biologically active molecules and pharmaceutical intermediates. Its unique structure and reactivity make it an important starting material in the synthesis of diverse heterocyclic compounds.Additionally, 3-Methylbenzofuran-2-carboxylic acid can serve as a key component in the production of advanced materials such as liquid crystals and polymers. Its ability to undergo various chemical transformations, including derivatization and functionalization, enables its incorporation into complex molecular frameworks with tailored properties.Furthermore, this compound is utilized in the development of novel catalysts and ligands for organic reactions, particularly in asymmetric synthesis. Its presence in the molecular structure imparts specific steric and electronic effects that can influence the outcome of chemical transformations, making it a valuable tool in the hands of synthetic chemists.