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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)-

Butanoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2R)-

CC[C@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: Butanoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2R)-
CAS Number: 170642-27-0
Product Number: AG0078J2(AGN-PC-0O4TP0)
Synonyms:
MDL No:
Molecular Formula: C19H19NO4
Molecular Weight: 325.3585

Identification/Properties

Computed Properties
Molecular Weight:
325.364g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
325.131g/mol
Monoisotopic Mass:
325.131g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
444
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


Fmoc-D-Abu-OH is a crucial reagent in chemical synthesis, particularly in peptide synthesis. With its ability to protect the amine group of amino acids, Fmoc-D-Abu-OH serves as a key building block in the assembly of complex peptide structures. By selectively masking the reactive amine, this reagent enables precise control over the sequence and functionality of peptides during synthesis. Its compatibility with solid-phase peptide synthesis makes it an indispensable tool for researchers and chemists alike seeking to create custom peptide sequences for various applications in drug discovery, biotechnology, and beyond.