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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)-

Benzeneacetic acid, a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(aR)-

O=C(N[C@H](c1ccccc1)C(=O)O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: Benzeneacetic acid, a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(aR)-
CAS Number: 111524-95-9
Product Number: AG00HC61(AGN-PC-0P269U)
Synonyms:
MDL No:
Molecular Formula: C23H19NO4
Molecular Weight: 373.4013

Identification/Properties

Computed Properties
Molecular Weight:
373.408g/mol
XLogP3:
4.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
373.131g/mol
Monoisotopic Mass:
373.131g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
537
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-H413
Precautionary Statements:
P261-P273-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-N-Fmoc-phenylglycine is a valuable building block in chemical synthesis, particularly in the field of peptide and protein chemistry. This compound is commonly used as a chiral auxiliary, providing a means to introduce chirality into molecules during synthesis. Its application in peptide chemistry allows for the controlled assembly of complex peptides with specific spatial arrangements of amino acid residues. By incorporating (R)-N-Fmoc-phenylglycine into peptide structures, chemists can manipulate the stereochemistry of the resulting peptides, which is crucial for their biological activity and function. Additionally, the Fmoc protecting group facilitates the stepwise solid-phase peptide synthesis by enabling selective deprotection and coupling reactions. The versatility and utility of (R)-N-Fmoc-phenylglycine make it an essential tool for chemists working on the synthesis of bioactive peptides and proteins.