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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-Phenylalanine,4-bromo-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-

O=C(N[C@@H](C(=O)O)Cc1ccc(cc1)Br)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: D-Phenylalanine,4-bromo-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
CAS Number: 198545-76-5
Product Number: AG002BLV(AGN-PC-0QPYHZ)
Synonyms:
MDL No: MFCD00273459
Molecular Formula: C24H20BrNO4
Molecular Weight: 466.3239

Identification/Properties

Properties
MP:
170-172 °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:
584
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


The (R)-N-Fmoc-4-Bromophenylalanine is a highly valuable and versatile compound used in chemical synthesis. Its application in organic synthesis lies in its ability to serve as a key building block in peptide and protein chemistry. By incorporating (R)-N-Fmoc-4-Bromophenylalanine into peptide sequences, chemists can introduce specific functionality and structural modifications to peptides, which can have implications in various biological and pharmaceutical studies. Its unique structure and reactivity make it a sought-after reagent for creating peptide analogs, studying protein structure-function relationships, and developing new drug candidates with improved properties and activities.