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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-Tyrosine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-2-propenyl-

C=CCOc1ccc(cc1)C[C@@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: L-Tyrosine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-2-propenyl-
CAS Number: 146982-30-1
Product Number: AG003QO6(AGN-PC-0O3F26)
Synonyms:
MDL No:
Molecular Formula: C27H25NO5
Molecular Weight: 443.4911

Identification/Properties

Properties
MP:
140-142 °C
BP:
668.7±55.0 °C(Predicted)
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
443.499g/mol
XLogP3:
5.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
10
Exact Mass:
443.173g/mol
Monoisotopic Mass:
443.173g/mol
Topological Polar Surface Area:
84.9A^2
Heavy Atom Count:
33
Formal Charge:
0
Complexity:
651
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)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(allyloxy)phenyl)propanoic acid, also known as $name$, is a versatile compound widely employed in chemical synthesis as a chiral building block. Its enantiopure form allows for precise control over the stereochemistry of reactions, making it a valuable tool in the synthesis of complex organic molecules. In chemical synthesis, (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(allyloxy)phenyl)propanoic acid is particularly useful in the creation of asymmetric catalysts, chiral ligands, and pharmaceutical intermediates. The presence of the fluorenyl group enhances the stability and reactivity of the compound, enabling it to participate in various key synthetic transformations.Additionally, the allyloxy and phenyl moieties present in the structure offer diverse functionalization possibilities, allowing for further structural modifications to tailor the compound for specific synthetic pathways. Through strategic use of (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(allyloxy)phenyl)propanoic acid, chemists can streamline reaction sequences, improve stereocontrol, and access novel chemical entities with high enantiomeric purity.