CAS 200336-86-3
:Fmoc-Asp(2-phenylisopropyl ester)-OH
Description:
Fmoc-Asp(2-phenylisopropyl ester)-OH is a chemical compound commonly used in peptide synthesis and research. It is a derivative of aspartic acid, where the amino group is protected by a 9-fluorenylmethoxycarbonyl (Fmoc) group, which is a widely used protective group in solid-phase peptide synthesis. The presence of the 2-phenylisopropyl ester indicates that the carboxylic acid group of aspartic acid is esterified, enhancing its lipophilicity and potentially influencing its reactivity and solubility in organic solvents. This compound typically appears as a white to off-white solid and is soluble in organic solvents like dichloromethane and dimethylformamide. Its structure allows for selective deprotection of the Fmoc group under mild basic conditions, facilitating the stepwise assembly of peptides. The compound is utilized in various biochemical applications, including drug development and the study of protein interactions, due to its ability to mimic natural amino acids while providing unique chemical properties.
Formula:C28H27NO6
Synonyms:- Fmoc-Asp(2-phenylisopropylester)-OH
- Fmoc-Asp(O-2-Phipr)-Oh
- FMOC-ASP(O-2-PHIPR)-OH USP/EP/BP
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID BETA-2-PHENYLISOPROPYL ESTER
- (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-4-(2-phenylpropan-2-yloxy)butanoic acid
- N-Fmoc-L-aspartic acid 4-(2-phenyl-2-propyl) ester
- FMOC-ASP(2-PHENYLISOPROPYL ESTER)-OH
- FMoc-Asp(OPp)-OH
- (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-oxo-4-((2-phenylpropan-2-yl)oxy)butanoic acid
- (9H-Fluoren-9-yl)MethOxy]Carbonyl Asp(OPis)-OH
- Fmoc-L-Asp(2-phenylisopropyloxy)-OH
- FMOC-ASP(OPIS)-OH
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID BETA-(1,1-DIMETHYL) BENZYL ESTER
- N-ALPHA-FMOC-L-ASPARTIC ACID BETA-2-PHENYLISOPROPYL ESTER
- FMOC-ASP[BZL(ME2)]-OH
- FMOC-ASPARTIC ACID(2-PHENYLISOPROPYL ESTER)
- Fmoc-L-Asp(PP)-OH
- Fmoc-L-aspartic acid β-2-phenylisopropyl ester≥ 99% (HPLC, Chiral purity)
- Fmoc-L-aspartic acid β-2-phenylisopropyl ester
- L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(1-methyl-1-phenylethyl) ester
- FMOC-L-ASPARTIC ACID BETA-2-PHENYLISOPROPYL ESTER
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Found 6 products.
Fmoc-Asp(2-phenylisopropyl ester)-OH
CAS:An aspartic acid derivative allowing specific side chain deprotection with 1% TFA in dichloromethane. Ocampo et al. applied OPp protection during the synthesis of a peptide-oligonucleotide conjugate and cleaved it with 3% trichloroacetic acid in DCM. The OPp derivative is far less prone towards base-catalyzed aspartimide formation than the OAll, OBzl, or ODmab esters, its stability comes close to the stability of the OtBu ester.Formula:C28H27NO6Purity:99.53%Color and Shape:White PowderMolecular weight:473.53L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(1-methyl-1-phenylethyl) ester
CAS:Formula:C28H27NO6Purity:97%Color and Shape:SolidMolecular weight:473.5171Fmoc-L-aspartic acid β-2-phenylisopropyl ester
CAS:Formula:C28H27NO6Purity:≥ 99%Color and Shape:White to off-white powderMolecular weight:473.52Fmoc-L-aspartic acid beta-2-phenylisopropyl ester
CAS:<p>Fmoc-L-aspartic acid beta-2-phenylisopropyl ester is a macrocyclic amino acid with conformational and anti-inflammatory properties. It has been shown to inhibit the proliferation of cancer cells in vitro, as well as the osteolytic, lymphoproliferative, and inflammatory activities in vivo. Fmoc-L-aspartic acid beta-2-phenylisopropyl ester also has antiarrhythmic effects on cardiac tissue that are caused by its ability to bind to chloride channels. This compound also inhibits the production of inflammatory cytokines such as tumor necrosis factor alpha (TNFα) and interleukin 6 (IL6).</p>Formula:C28H27NO6Purity:Min. 95%Color and Shape:PowderMolecular weight:473.52 g/mol(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-oxo-4-((2-phenylpropan-2-yl)oxy)butanoic acid
CAS:Purity:97%Molecular weight:473.5249939





