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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)-

1,2-Benzenedicarboxylic acid, 4-[(R)-aminocarboxymethyl]-

N[C@H](c1ccc(c(c1)C(=O)O)C(=O)O)C(=O)O Request for Quotation
Chemical Name: 1,2-Benzenedicarboxylic acid, 4-[(R)-aminocarboxymethyl]-
CAS Number: 201730-10-1
Product Number: AG0027T4(AGN-PC-0O755N)
Synonyms:
MDL No: MFCD03453633
Molecular Formula: C10H9NO6
Molecular Weight: 239.1816

Identification/Properties

Computed Properties
Molecular Weight:
239.183g/mol
XLogP3:
-2.7
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
4
Exact Mass:
239.043g/mol
Monoisotopic Mass:
239.043g/mol
Topological Polar Surface Area:
138A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
342
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


1,2-Benzenedicarboxylic acid, 4-[(R)-aminocarboxymethyl]- is a versatile compound utilized in various chemical synthesis applications. Due to its unique structure, this compound serves as a key building block in the synthesis of a wide range of advanced materials and pharmaceuticals. Its primary function lies in its ability to participate in complex organic reactions, facilitating the creation of structurally diverse molecules with specific chirality preferences. When incorporated into chemical synthesis processes, 1,2-Benzenedicarboxylic acid, 4-[(R)-aminocarboxymethyl]- enables precise control over stereochemistry, leading to the production of highly pure and stable compounds with targeted properties. Its successful application in the synthesis of key intermediates and active pharmaceutical ingredients highlights its importance in the modern chemistry landscape. By harnessing the capabilities of this compound, researchers and professionals can achieve remarkable advancements in the development of novel materials and therapeutic agents, paving the way for innovative solutions in various industries.