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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-amino-4-[(2-methylpropan-2-yl)oxycarbonylamino]benzoic acid

O=C(OC(C)(C)C)Nc1ccc(cc1N)C(=O)O Request for Quotation
Chemical Name: 3-amino-4-[(2-methylpropan-2-yl)oxycarbonylamino]benzoic acid
CAS Number: 954238-52-9
Product Number: AG00IJ2Q(AGN-PC-03Y37C)
Synonyms:
MDL No:
Molecular Formula: C12H16N2O4
Molecular Weight: 252.26644

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335-H412
Precautionary Statements:
P261-P273-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 3-Amino-4-((tert-butoxycarbonyl)amino)benzoic acid is a valuable organic compound commonly utilized as a building block in the creation of various bioactive molecules. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other complex organic compounds due to its versatile nature and reactivity in organic reactions.Specifically, this compound is often employed in peptide synthesis as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group attached to the amino group serves as a protective group during peptide assembly, allowing for selective deprotection and functional group manipulation at specific stages of the synthesis. This Boc-protected amino acid is crucial in the construction of peptide chains, enabling the precise control of peptide sequence and structure.Furthermore, the presence of the amino and carboxylic acid functional groups in 3-Amino-4-((tert-butoxycarbonyl)amino)benzoic acid facilitates its involvement in amidation reactions, esterifications, and other synthetic transformations. These reactions enable the incorporation of this compound into various organic frameworks, enhancing its utility in the construction of diverse chemical entities with specific functionalities.Overall, 3-Amino-4-((tert-butoxycarbonyl)amino)benzoic acid plays a crucial role in chemical synthesis by serving as a versatile building block for the creation of complex molecules, particularly in the fields of pharmaceutical and agrochemical research. Its strategic use in peptide synthesis and other organic reactions highlights its significance as a key component in the design and development of novel bioactive compounds.