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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, monopotassium salt

OC(=O)C[C@@H](C(=O)[O-])N.[K+] Request for Quotation
Chemical Name: L-Aspartic acid, monopotassium salt
CAS Number: 1115-63-5
Product Number: AG0035I2(AGN-PC-0P27F8)
Synonyms:
MDL No:
Molecular Formula: C4H6KNO4
Molecular Weight: 171.1930

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
20.5 ° (C=8, 6mol/L HCl)
Computed Properties
Molecular Weight:
171.193g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
170.993g/mol
Monoisotopic Mass:
170.993g/mol
Topological Polar Surface Area:
103A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
137
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


L-Aspartic acid potassium salt is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a crucial reagent for the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to act as a chiral building block makes it highly valuable in the synthesis of complex molecules and asymmetric catalysis. Additionally, L-Aspartic acid potassium salt finds application in the production of polymers, resins, and surfactants, where its functional groups contribute to the desired properties of the final products. Its compatibility with a range of solvents and reaction conditions further enhances its utility in synthetic processes, making it a preferred choice for researchers and chemists involved in the development of novel compounds and materials.