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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)-

Propanoic acid, 2-hydroxy-, monosodium salt, (2R)-

[O-]C(=O)[C@H](O)C.[Na+] Request for Quotation
Chemical Name: Propanoic acid, 2-hydroxy-, monosodium salt, (2R)-
CAS Number: 920-49-0
Product Number: AG003UCB(AGN-PC-0VXVB6)
Synonyms:
MDL No:
Molecular Formula: C3H5NaO3
Molecular Weight: 112.0598

Identification/Properties

Computed Properties
Molecular Weight:
112.06g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
112.014g/mol
Monoisotopic Mass:
112.014g/mol
Topological Polar Surface Area:
60.4A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
63.2
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Sodium D-lactate, a chemical compound often used in chemical synthesis, serves as a versatile ingredient in various applications. Its utility lies in its ability to act as a chiral building block, particularly in the production of pharmaceuticals and fine chemicals. Due to its specific stereochemistry, Sodium D-lactate can be employed as a key component in the creation of enantiomerically pure compounds, crucial for enhancing the efficacy and safety of many medications. Furthermore, its role as a precursor in the synthesis of complex organic molecules makes it invaluable in the development of new materials and compounds with diverse functionalities. In the realm of chemical synthesis, Sodium D-lactate emerges as a fundamental tool for researchers and professionals seeking to engineer precise and tailored molecular structures tailored to specific applications.