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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)-

L-Aspartic acid, potassium salt

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Chemical Name: L-Aspartic acid, potassium salt
CAS Number: 14007-45-5
Product Number: AG01DQ15(AGN-PC-0PP7CB)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


Potassium L-aspartate is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This amino acid derivative serves as a crucial building block in the creation of various pharmaceuticals, food additives, and specialty chemicals. When incorporated into organic reactions, Potassium L-aspartate acts as a chiral source, enabling the selective formation of enantiomerically pure products. Its ability to promote asymmetric synthesis makes it an invaluable tool for generating complex molecules with enhanced stereochemical control. Additionally, Potassium L-aspartate can participate in metal-catalyzed transformations, facilitating the construction of intricate molecular structures with high efficiency. Its compatibility with a diverse range of chemical processes further highlights its importance in the realm of synthetic organic chemistry.