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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)-

D-Norvaline

CCC[C@H](C(=O)O)N Request for Quotation
Chemical Name: D-Norvaline
CAS Number: 2013-12-9
Product Number: AG002DC5(AGN-PC-0O73TT)
Synonyms:
MDL No:
Molecular Formula: C5H11NO2
Molecular Weight: 117.1463

Identification/Properties

Properties
MP:
>300 °C(lit.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
-25 ° (C=10, 6mol/L HCl)
Computed Properties
Molecular Weight:
117.148g/mol
XLogP3:
-2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
117.079g/mol
Monoisotopic Mass:
117.079g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
82.5
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

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


D(-)-Norvaline is a chiral amino acid derivative that finds significant application in chemical synthesis. Due to its structural similarities to valine, D(-)-Norvaline can serve as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials. In organic chemistry, it is frequently used as a precursor in the synthesis of complex molecules and peptides. Its chirality imparts specific stereochemical properties to the synthesized compounds, making it an essential tool for creating enantioselective molecules with improved biological activity or targeted effects. In addition, D(-)-Norvaline can also be employed in the development of new catalysts and ligands for asymmetric synthesis reactions, showcasing its versatility in the field of chemical synthesis.