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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)-

b-D-Glucopyranosiduronic acid, 4-aminophenyl

OC(=O)[C@H]1O[C@@H](Oc2ccc(cc2)N)[C@@H]([C@H]([C@@H]1O)O)O Request for Quotation
Chemical Name: b-D-Glucopyranosiduronic acid, 4-aminophenyl
CAS Number: 21080-66-0
Product Number: AG002KZP(AGN-PC-0QXKF8)
Synonyms:
MDL No:
Molecular Formula: C12H15NO7
Molecular Weight: 285.2500

Identification/Properties

Properties
Storage:
-10 ℃;
Computed Properties
Molecular Weight:
285.252g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
3
Exact Mass:
285.085g/mol
Monoisotopic Mass:
285.085g/mol
Topological Polar Surface Area:
143A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
345
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
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


4-Aminophenyl β-D-glucuronide is a versatile compound widely utilized in chemical synthesis for its unique properties and applications. This compound serves as a crucial building block in organic chemistry reactions, facilitating the synthesis of various complex molecules and pharmaceutical compounds. In chemical synthesis, 4-Aminophenyl β-D-glucuronide acts as a key reagent in the creation of nitrogen-containing structures and biomolecules. Its amino group enables it to participate in diverse coupling reactions, forming new bonds and functional groups within a molecule. This characteristic makes it valuable for the construction of biologically active molecules and drug intermediates.Furthermore, the glucuronide moiety in 4-Aminophenyl β-D-glucuronide imparts water solubility and stability to the compound. This feature is particularly advantageous in drug development and formulation, where water solubility is often essential for drug bioavailability and efficacy. By incorporating this glucuronide derivative into a molecule, researchers can improve its pharmacokinetic properties and enhance its therapeutic potential.Overall, 4-Aminophenyl β-D-glucuronide plays a pivotal role in chemical synthesis by enabling the efficient construction of diverse chemical structures and enhancing the properties of biologically active molecules. Its versatility and utility make it a valuable tool for synthetic chemists and pharmaceutical researchers seeking to develop novel compounds with potential therapeutic applications.