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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)-

3-Oxoisoindoline-4-carboxylic acid

OC(=O)c1cccc2c1C(=O)N=C2 Request for Quotation
Chemical Name: 3-Oxoisoindoline-4-carboxylic acid
CAS Number: 935269-27-5
Product Number: AG00H32F(AGN-PC-0WAHTJ)
Synonyms:
MDL No:
Molecular Formula: C9H5NO3
Molecular Weight: 175.1409

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
177.159g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
177.043g/mol
Monoisotopic Mass:
177.043g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
251
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


3-Oxoisoindoline-4-carboxylic acid is a versatile compound widely used in chemical synthesis for its unique reactivity and structural properties. This compound serves as a key building block in organic chemistry, enabling the synthesis of various complex molecules through diverse reaction pathways. One prominent application of 3-Oxoisoindoline-4-carboxylic acid is its role as a precursor in the synthesis of biologically active compounds and pharmaceutical intermediates. It can undergo various chemical transformations such as acylation, alkylation, and condensation reactions to yield a wide range of functionalized products with tailored properties. Furthermore, the presence of the carbonyl group in its structure allows for further derivatization, leading to the creation of novel molecules with enhanced activity or selectivity. In addition to its use in pharmaceutical chemistry, 3-Oxoisoindoline-4-carboxylic acid also finds applications in materials science, agrochemicals, and other industries requiring the construction of complex organic scaffolds. Its versatility and importance in chemical synthesis make it a valuable tool for researchers and professionals seeking to access diverse molecular architectures for various applications.