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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-Phenylalanine,3-bromo-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-

O=C(N[C@H](C(=O)O)Cc1cccc(c1)Br)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: L-Phenylalanine,3-bromo-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
CAS Number: 220497-48-3
Product Number: AG0034XP(AGN-PC-0QYLQF)
Synonyms:
MDL No:
Molecular Formula: C24H20BrNO4
Molecular Weight: 466.3239

Identification/Properties

Properties
MP:
144.2 °C
BP:
660.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
1.6500 (estimate)
Computed Properties
Molecular Weight:
466.331g/mol
XLogP3:
5.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
465.058g/mol
Monoisotopic Mass:
465.058g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
592
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:
H302-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


Fmoc-3-bromo-L-phenylalanine is a versatile amino acid derivative commonly employed in peptide synthesis for its unique chemical properties. This compound serves as a valuable building block in the construction of peptide sequences due to its ability to selectively react with amines and other nucleophiles. By harnessing the reactivity of the bromine atom, Fmoc-3-bromo-L-phenylalanine enables precise control over the regioselectivity of peptide bond formation, facilitating the synthesis of complex peptide structures with high purity and efficiency. Furthermore, the Fmoc protecting group confers additional stability against undesired side reactions, allowing for strategic deprotection steps to be carried out in a controlled manner. As a key component in modern peptide chemistry, Fmoc-3-bromo-L-phenylalanine plays a crucial role in the synthesis of bioactive peptides, pharmaceutical compounds, and peptidomimetics with tailored properties and functionalities.