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CAS 201473-90-7

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Fmoc-Dap(Fmoc)-OH

Description:
Fmoc-Dap(Fmoc)-OH, also known as Fmoc-protected 2,3-diaminopropanoic acid, is a chemical compound commonly used in peptide synthesis and research. It features a fluorenylmethyloxycarbonyl (Fmoc) protective group, which is widely utilized in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The presence of two amino groups in its structure allows for the formation of various peptide linkages, making it versatile for constructing complex peptides. The compound is typically a white to off-white solid and is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. Its molecular structure contributes to its reactivity and functionality in synthetic applications. Safety precautions should be observed when handling this compound, as with many chemical substances, to avoid potential hazards. Overall, Fmoc-Dap(Fmoc)-OH is an important building block in the field of organic chemistry and biochemistry, particularly in the synthesis of peptides and related compounds.
Formula:C33H28N2O6
InChI:InChI=1/C33H28N2O6/c36-31(37)30(35-33(39)41-19-29-26-15-7-3-11-22(26)23-12-4-8-16-27(23)29)17-34-32(38)40-18-28-24-13-5-1-9-20(24)21-10-2-6-14-25(21)28/h1-16,28-30H,17-19H2,(H,34,38)(H,35,39)(H,36,37)/t30-/m0/s1
InChI key:CEEGOSWFFHSPHM-PMERELPUSA-N
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=NC[C@@H](C(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12)O
Synonyms:
  • N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-L-alanine
  • N-ALPHA,N-BETA-DI-FMOC-(S)-2,3-DIAMINOPROPIONIC ACID
  • 201473-90-7
  • Nalpha-Fmoc-3-(Fmoc-amino)-L-alanine
  • N
  • Nα,β-Bis-Fmoc-L-2,3-diaminopropionic acid
  • FMOC-DAP(FMOC)-OH USP/EP/BP
  • FMoc-Dap(FMoc)-OH(Na,N3-diFMoc-2,3-DiaMinopropionic acid)
  • N-a,N-di-Fmoc-L-2,3-diaminopropionicacid
  • Fmoc-3-(Fmoc-amino)-L-alanine, Nα,Nβ-di-Fmoc-L-2,3-diaminopropionic acid
  • See more synonyms
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