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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)-

1H-Indole-2,5-dicarboxylic acid

OC(=O)c1ccc2c(c1)cc([nH]2)C(=O)O Request for Quotation
Chemical Name: 1H-Indole-2,5-dicarboxylic acid
CAS Number: 117140-77-9
Product Number: AG000DSU(AGN-PC-0L8XJJ)
Synonyms:
MDL No:
Molecular Formula: C10H7NO4
Molecular Weight: 205.1669

Identification/Properties

Computed Properties
Molecular Weight:
205.169g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
205.038g/mol
Monoisotopic Mass:
205.038g/mol
Topological Polar Surface Area:
90.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
291
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Indole-2,5-dicarboxylic acid, chemically known as C10H7NO4, serves as a versatile building block in chemical synthesis. With its unique structure and reactivity, this compound finds wide application in the creation of various pharmaceuticals, agrochemicals, and functional materials. In organic synthesis, 1H-Indole-2,5-dicarboxylic acid can undergo a range of transformations, such as esterification, amidation, or cyclization reactions, to generate diverse intermediates and final products. These products may exhibit a broad spectrum of biological activities, including antimicrobial, antiviral, or anticancer properties, making this compound a valuable tool in drug discovery and development. Additionally, 1H-Indole-2,5-dicarboxylic acid can be utilized in the preparation of functionalized polymers, dyes, or liquid crystals, showcasing its utility in material science. Overall, the strategic incorporation of 1H-Indole-2,5-dicarboxylic acid in synthetic pathways enables the efficient and controlled construction of complex molecular architectures with tailored properties and functionalities.