8.52086
Fmoc-Asp(O-2-PhiPr)-OH
≥97% (TLC), for peptide synthesis, Novabiochem®
Manufacturer: Sigma Aldrich
CAS Number: 200336-86-3
Synonym(S): Fmoc-Asp(O-2-PhiPr)-OH, N-α-Fmoc-L-aspartic acid β-2-phenylisopropyl ester
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | 8.52086-1-G | In Stock | ₹ 16,000.01 |
| 5 G | 8.52086-5-G | In Stock | ₹ 66,490.00 |
8.52086 - 1 G
In Stock
Quantity
1
Base Price: ₹ 16,000.01
GST (18%): ₹ 2,880.002
Total Price: ₹ 18,880.012
product name
Fmoc-Asp(O-2-PhiPr)-OH, Novabiochem®
Quality Level
200
product line
Novabiochem®
Assay
≥93.0% (acidimetric)≥95.0% (HPLC)≥97% (TLC)
form
powder
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
manufacturer/tradename
Novabiochem®
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
15-25°C
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Chem-Impex International, Inc. Fmoc-L-aspartic acid b-2-phenylisopropyl ester | 200336-86-3 | MFCD00237012 | 1G | -- | ₹ 20,966.48 | |
| | STA PHARMACEUTICAL US LLC WuXi TIDES Fmoc-L-Asp(O-2-PhiPr)-OH | 200336-86-3, 10GR | -- | ₹ 1,11,056.88 | |
| | STA PHARMACEUTICAL US LLC WuXi TIDES Fmoc-L-Asp(O-2-PhiPr)-OH | 200336-86-3, 100GR | -- | ₹ 7,09,630.36 | |
| | STA PHARMACEUTICAL US LLC WuXi TIDES Fmoc-L-Asp(O-2-PhiPr)-OH | 200336-86-3, 1GR | -- | ₹ 17,503.86 | |
| | STA PHARMACEUTICAL US LLC WuXi TIDES Fmoc-L-Asp(O-2-PhiPr)-OH | 200336-86-3, 50GR | -- | ₹ 4,15,318.51 | |
| | STA PHARMACEUTICAL US LLC WuXi TIDES Fmoc-L-Asp(O-2-PhiPr)-OH | 200336-86-3, 5GR | -- | ₹ 65,523.56 | |
| | Fmoc-Asp(O-2-PhiPr)-OH | -- | ₹ 6,331.44 - ₹ 1,16,104.92 | |
| | (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-oxo-4-((2-phenylpropan-2-yl)oxy)butanoic acid | -- | ₹ 7,187.04 - ₹ 65,538.96 |
Related Products
Description
- General description: Quasi-orthogonally-protected Asp derivative.The 2-PhiPr group can be removed selectively in the presence of tBu-based protecting groups by treatment with 1% TFA in DCM [1], making this derivative an extremely useful tool for the preparation of cyclic peptides by Fmoc SPPS [2] or for library synthesis. For the on-resin synthesis of side-chain to side-chain lactam bridged peptides, the combination of Lys(Mtt) and Asp(O-2-PhiPr) is particularly advantageous since both side-chains can be simultaneously unmasked in a single step.This derivative has also been used in solution to prepare bicyclic helix initiating peptides [3]. Associated Protocols and Technical ArticlesCleavage and Deprotection Protocols for Fmoc SPPSLiterature references[1] C. Yue, et al. (1993) Tetrahedron Lett., 34, 323. [2] F. Dick, et al. in ′Peptides 1996, Proc. of 24th European Peptide Symposium′, R. Ramage & R. Epton (Eds), Mayflower Scientific Ltd., Birmingham, 1998, pp. 339. [3] J. W. Taylor, et al., Poster 185 presented at the American Peptide Symposium, San Diego, 2001.
- Linkage: Replaces: 04-12-1200
- Analysis Note: Color (visual): white to slight yellow to beigeAppearance of substance (visual): powderIdentity (IR): passes testEnantiomeric purity: ≥ 99.0 % (a/a)Purity (TLC(011A)): ≥ 97 %Purity (TLC(0811)): ≥ 97 %Assay (HPLC, area%): ≥ 95.0 % (a/a)Solubility (1 mmole in 2 ml DMF): clearly solubleAssay (acidimetric): ≥ 93.0 %Water (K. F.): ≤ 2.0 %To see the solvent systems used for TLC of Novabiochem® products please click here.
- Legal Information: Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany
SAFETY INFORMATION
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable