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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-Benzofurancarboxylicacid, 7-chloro-3-methyl-

OC(=O)c1oc2c(c1C)cccc2Cl Request for Quotation
Chemical Name: 2-Benzofurancarboxylicacid, 7-chloro-3-methyl-
CAS Number: 32565-18-7
Product Number: AG00CRA4(AGN-PC-0KEKWR)
Synonyms:
MDL No:
Molecular Formula: C10H7ClO3
Molecular Weight: 210.6138

Identification/Properties

Computed Properties
Molecular Weight:
210.613g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
210.008g/mol
Monoisotopic Mass:
210.008g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
244
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


7-Chloro-3-methylbenzofuran-2-carboxylic acid, also known as $name$, is a versatile compound that plays a crucial role in chemical synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique molecular structure makes it highly valuable in the development of novel compounds with diverse applications in the field of chemistry.One of the primary uses of 7-Chloro-3-methylbenzofuran-2-carboxylic acid is in the synthesis of heterocyclic compounds. By incorporating this compound into chemical reactions, chemists can access a wide range of structurally complex molecules that exhibit specific biological activities or desirable properties. Its presence in a synthetic pathway can facilitate the formation of new bonds, enable the introduction of functional groups, and influence the overall reactivity of the reaction.Additionally, 7-Chloro-3-methylbenzofuran-2-carboxylic acid serves as a valuable precursor for the synthesis of various drug candidates. Its incorporation into pharmaceutical molecules can enhance their stability, bioavailability, and pharmacological properties. By strategically incorporating this compound into the molecular structure of drugs, researchers can fine-tune their efficacy and optimize their therapeutic potential.Overall, the application of 7-Chloro-3-methylbenzofuran-2-carboxylic acid in chemical synthesis offers chemists a powerful tool for the design and production of novel compounds with diverse functionalities. Its versatility and reactivity make it an indispensable component in the development of cutting-edge molecules with significant implications for the fields of medicinal chemistry, materials science, and beyond.