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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, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-,(2S)-

O=C(OCC1c2ccccc2c2c1cccc2)NC[C@@H](C(=O)O)C Request for Quotation
Chemical Name: Propanoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-,(2S)-
CAS Number: 203854-58-4
Product Number: AG00294S(AGN-PC-0QU2GG)
Synonyms:
MDL No:
Molecular Formula: C19H19NO4
Molecular Weight: 325.3585

Identification/Properties

Properties
BP:
555.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
325.364g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
325.131g/mol
Monoisotopic Mass:
325.131g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
444
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


(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpropanoic acid, also known as "$name$", is a valuable compound widely employed in chemical synthesis due to its chiral nature and versatile reactivity. In chemical synthesis, $name$ serves as a crucial building block for the creation of complex molecules with precise stereochemistry. Its chiral center and unique structural features make it a preferred reagent in the asymmetric synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Specifically, $name$ can be utilized as a key intermediate in the production of peptides and peptidomimetics, where its chiral backbone imparts desired stereochemical properties to the final molecules. Additionally, its methoxy carbonyl group offers protection to reactive functional groups during synthetic transformations, enabling selective manipulations and controlled reactions.Moreover, the presence of the fluorenyl moiety in $name$ enhances the stability and rigidity of the molecule, making it an ideal substrate for challenging synthetic transformations that require a robust and structurally defined scaffold. Overall, the application of (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpropanoic acid in chemical synthesis contributes significantly to the efficient and precise construction of complex molecules in modern organic chemistry.