CAS 118476-89-4

Fmoc-D-Orn(Boc)-OH

Description:

Fmoc-D-Orn(Boc)-OH, with the CAS number 118476-89-4, is a protected amino acid derivative commonly used in peptide synthesis. It features a D-ornithine backbone, which is an essential building block in the formation of peptides. The Fmoc (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective reactions during synthesis. The Boc (tert-butyloxycarbonyl) group protects the side chain amine, enhancing the stability and reactivity of the molecule. This compound is typically white to off-white in appearance and is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. Fmoc-D-Orn(Boc)-OH is utilized in solid-phase peptide synthesis (SPPS) due to its compatibility with various coupling reagents and its ability to facilitate the formation of peptide bonds. Its structural features make it valuable in the development of peptides with specific biological activities, including those used in drug design and therapeutic applications.

Formula: C₂₅H₃₀N₂O₆

InChI: InChI=1/C25H30N2O6/c1-25(2,3)33-23(30)26-14-8-13-21(22(28)29)27-24(31)32-15-20-18-11-6-4-9-16(18)17-10-5-7-12-19(17)20/h4-7,9-12,20-21H,8,13-15H2,1-3H3,(H,26,30)(H,27,31)(H,28,29)/t21-/m1/s1

InChI key: JOOIZTMAHNLNHE-OAQYLSRUSA-N

SMILES: CC(C)(C)OC(=NCCC[C@H](C(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12)O

Synonyms:

• (2R)-5-(tert-butoxycarbonylamino)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoic acid
• N-Fmoc-N’-Boc-D-Ornithine
• FMOC-(N-DELTA-BOC)-D-ORNITHINE
• N-ALPHA-FMOC-N-D-T-BOC-D-ORNITHINE
• Ndelta-Boc-Nalpha-Fmoc-D-ornithine
• 9-fluorenylmethoxycarbonyl-L-ornithine-tert-butoxycarbonyl
• Nα-Fmoc-Nδ-Boc-D-ornithine≥ 99% (HPLC)
• Fmoc-D-Orn(Boc)-OH, ≥98%
• Fmoc-(Nd-Boc)-D-ornithine
• FMOC-D-ORN(BOC)-OH
• N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-DELTA-T-BUTOXYCARBONYL-D-ORNITHINE
• Fmoc-(N'-Boc)-D-ornithine
• Nα-Fmoc-Nδ-Boc-D-ornithine
• D-Ornithine, N5-[(1,1-dimethylethoxy)carbonyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-
• Fmoc-D-Orn(Boc)-OH Novabiochem
• N-alpha-Fmoc-N-delta-Boc-D-ornithine
• REF DUPL: N-alpha-Fmoc-N-delta-Boc-D-ornithine
• N5-Boc-N2-Fmoc-D-ornithine
• N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-delta-t-butyloxycarbonyl-D-ornithine
• (9H-Fluoren-9-yl)MethOxy]Carbonyl D-Orn(Boc)-OH
• N-ALPHA-FMOC-N-DELTA-T-BOC-D-ORNITHINE
• N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-GAMMA-(T-BUTYLOXYCARBONYL)-D-ORNITHINE
• (R)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-5-((tert-butoxycarbonyl)aMino)pentanoic acid
• (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
• (2R)-5-{[(tert-butoxy)carbonyl]amino}-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoic acid
• N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-DELTA-TERT-BUTYLOXYCARBONYL-D-ORNITHINE
• Fmoc-D-Orn(Boc)
• FMOC-D-ORNITHINE(BOC)-OH
• N^d-Boc-N^a-FMoc-D-ornithine, 95%

Nδ-Boc-Nα-Fmoc-D-ornithine, 95%

CAS: 118476-89-4

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₂₅H₃₀N₂O₆

Purity: 95%

Molecular weight: 454.52

Ref: 02-H62930

Fmoc-D-Orn(Boc)-OH

CAS: 118476-89-4

Purity: 97%

Color and Shape: Solid

Molecular weight: 454.21

Ref: 10-F551648

Fmoc-D-Orn(Boc)-OH

CAS: 118476-89-4

Formula: C₂₅H₃₀N₂O₆

Purity: 98%

Color and Shape: Solid

Molecular weight: 454.5155

Ref: IN-DA0076CG

Fmoc-D-Orn(Boc)-OH

CAS: 118476-89-4

Fmoc-D-Orn(Boc)-OH

Formula: C₂₅H₃₀N₂O₆

Purity: >98%

Color and Shape: Solid

Molecular weight: 454.52

Ref: 54-OR1013351

Fmoc-D-Orn(Boc)-OH

CAS: 118476-89-4

Fmoc-D-Orn(Boc)-OH

Formula: C₂₅H₃₀N₂O₆

Purity: 96%

Molecular weight: 454.52

Ref: IN-DG131117

N-alpha-Fmoc-N-delta-Boc-D-ornithine

CAS: 118476-89-4

N-alpha-Fmoc-N-delta-Boc-D-ornithine (NFDO) is an antibiotic that belongs to the group of macrocyclic, cyclic antibiotics. This drug has antibacterial activity against gram-negative pathogens and is most effective against E. coli. NFDO is synthesized by a solid phase synthesis that occurs in two stages: first, FMOC protected amino acids are coupled to the resin and then deprotection is carried out with piperidine in DMF at room temperature. The final product is obtained by cleavage of the peptide from the resin with trifluoroacetic acid and purification by HPLC.

Formula: C₂₅H₃₀N₂O₆

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 454.52 g/mol

Ref: 3D-FF47771

Fmoc-D-Orn(Boc)-OH

CAS: 118476-89-4

Bachem ID: 4004451.

Formula: C₂₅H₃₀N₂O₆

Purity: 99.5%

Color and Shape: White

Molecular weight: 454.52

Ref: 01-4004451