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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)-

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

O=C(N[C@@H](C(=O)O)Cc1ccncc1)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: 4-Pyridinepropanoic acid,a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (aR)-
CAS Number: 205528-30-9
Product Number: AG002A5R(AGN-PC-0QVDNM)
Synonyms:
MDL No:
Molecular Formula: C23H20N2O4
Molecular Weight: 388.4159

Identification/Properties

Properties
BP:
646.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
388.423g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
388.142g/mol
Monoisotopic Mass:
388.142g/mol
Topological Polar Surface Area:
88.5A^2
Heavy Atom Count:
29
Formal Charge:
0
Complexity:
555
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
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-D-4-Pal-OH is a valuable building block in chemical synthesis, particularly in peptide chemistry. It serves as a versatile amino acid derivative that can be used in the solid-phase peptide synthesis (SPPS) process. By incorporating Fmoc-D-4-Pal-OH into a peptide sequence, chemists can introduce specific properties or functionalities to the resulting peptide molecules, thus enhancing their potential applications in various fields such as drug discovery, biomedical research, and materials science. As a protected amino acid, Fmoc-D-4-Pal-OH enables precise control over the sequence and structure of peptides, making it an essential tool for designing and synthesizing custom peptides with desired properties and functions. Its compatibility with standard peptide synthesis protocols and ease of deprotection make Fmoc-D-4-Pal-OH a popular choice for chemists striving to create novel peptides with enhanced bioactivity and stability.