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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)-

Benzoic acid, 4-[[(2,5-dihydroxyphenyl)methyl]amino]-, methyl ester

COC(=O)c1ccc(cc1)NCc1cc(O)ccc1O Request for Quotation
Chemical Name: Benzoic acid, 4-[[(2,5-dihydroxyphenyl)methyl]amino]-, methyl ester
CAS Number: 140674-76-6
Product Number: AG001COK(AGN-PC-0JK643)
Synonyms:
MDL No:
Molecular Formula: C15H15NO4
Molecular Weight: 273.2839

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Solubility:
DMSO: soluble
Computed Properties
Molecular Weight:
273.288g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
273.1g/mol
Monoisotopic Mass:
273.1g/mol
Topological Polar Surface Area:
78.8A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
315
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


In chemical synthesis, Benzoic acid, 4-[(2,5-dihydroxyphenyl)methylamino]-, methyl ester is commonly utilized as a versatile building block due to its unique structural properties. This compound serves as a key intermediate in the creation of various pharmaceuticals, agrochemicals, and functional materials. Its functional groups offer opportunities for the introduction of additional substituents, facilitating the synthesis of diverse molecules with tailored properties. The presence of both aromatic and amino moieties in its structure enables the formation of complex organic compounds through strategic conversions and modifications. Additionally, its methyl ester functionality provides a handle for further transformations, allowing for precise control over the chemical reactivity and properties of the final products.