1. Home
  2. 2-Naphthalenebutanoic acid,b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (bS)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

2-Naphthalenebutanoic acid,b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (bS)-

O=C(N[C@@H](Cc1ccc2c(c1)cccc2)CC(=O)O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: 2-Naphthalenebutanoic acid,b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (bS)-
CAS Number: 270063-40-6
Product Number: AG003CLI(AGN-PC-0R2WLI)
Synonyms:
MDL No:
Molecular Formula: C29H25NO4
Molecular Weight: 451.5131

Identification/Properties

Computed Properties
Molecular Weight:
451.522g/mol
XLogP3:
5.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
451.178g/mol
Monoisotopic Mass:
451.178g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
34
Formal Charge:
0
Complexity:
688
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

Request for Quotation

Customer Feedback

Chemical Structure


The (S)-3-(Fmoc-amino)-4-(2-naphthyl)butyric acid is a versatile compound widely utilized in chemical synthesis. Its application in organic chemistry primarily lies in peptide synthesis and solid-phase peptide synthesis. By incorporating this compound into the synthesis process, chemists can conveniently protect amino acids during peptide assembly, allowing for efficient and controlled formation of peptide bonds. This compound serves as a key intermediate in the production of various peptides and peptide-based molecules with specific biological activities. Furthermore, its unique structural features make it a valuable building block for designing and creating complex molecular structures in the field of medicinal chemistry and drug development.