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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)-

spiro[2H-indole-2,3-piperidine], 1,3-dihydro-

COc1cc(Br)cc2c1oc(c2)C(=O)O Request for Quotation
Chemical Name: spiro[2H-indole-2,3-piperidine], 1,3-dihydro-
CAS Number: 20037-37-0
Product Number: AG002CQ9(AGN-PC-0QRC24)
Synonyms:
MDL No:
Molecular Formula: C10H7BrO4
Molecular Weight: 271.0642

Identification/Properties

Computed Properties
Molecular Weight:
271.066g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
269.953g/mol
Monoisotopic Mass:
269.953g/mol
Topological Polar Surface Area:
59.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
258
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


5-Bromo-7-methoxybenzofuran-2-carboxylic acid is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a crucial building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its functional groups offer a platform for further derivatization, allowing chemists to tailor the molecule for specific applications.In organic synthesis, 5-Bromo-7-methoxybenzofuran-2-carboxylic acid can undergo various transformations such as esterification, amidation, and coupling reactions to create complex molecular structures. Its bromine substituent provides a handle for further functionalization, while the methoxy group imparts stability and can influence the compound's solubility and pharmacokinetic properties.Overall, the strategic placement of functional groups in 5-Bromo-7-methoxybenzofuran-2-carboxylic acid makes it a valuable intermediate in the synthesis of biologically active compounds and advanced materials, highlighting its significance in modern organic chemistry practices.