CAS 82911-69-1: N-(9-Fluorenylmethoxycarbonyloxy)succinimide
Formula:C19H15NO5
InChI:InChI=1S/C19H15NO5/c21-17-9-10-18(22)20(17)25-19(23)24-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16/h1-8,16H,9-11H2
InChI key:InChIKey=WMSUFWLPZLCIHP-UHFFFAOYSA-N
SMILES:C(OC(ON1C(=O)CCC1=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:- (2,5-Dioxopyrrolidin-1-yl) 9H-fluoren-9-ylmethyl carbonate
- (9H-Fluoren-9-yl)methyl succinimidyl carbonate
- (Fluorenylmethoxycarbonyl)hydroxysuccinimide ester
- 1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione
- 1-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]oxy]pyrrolidine-2,5-dione
- 1-{[(9H-fluoren-9-ylmethoxy)carbonyl]oxy}pyrrolidine-2,5-dione
- 2,5-Dioxopyrrolidin-1-yl (9H-fluoren-9-yl)methyl carbonate
- 2,5-Pyrrolidinedione, 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]oxy]-
- 9-Fluorenylmethyl N-succinimidyl carbonate
- 9-Fluorenylmethyl succinimidyl carbonate
- 9-Fluorenylmethyl-N-hydroxysuccinimide
- See more synonyms
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Found 13 products.
N-(9-Fluorenylmethoxycarbonyloxy)succinimide
CAS:Formula:C19H15NO5Purity:98%Color and Shape:SolidMolecular weight:337.3261Ref: IN-DA0034XN
10g21.00€1kg154.00€25g25.00€5kg553.00€100g36.00€10kgTo inquire250g69.00€25kgTo inquire500g99.00€Fmoc-OSu
CAS:Fmoc-OSu is a matrix that can be used as an absorption enhancer in biological and biochemical studies. The ester hydrochloride form of Fmoc-OSu is soluble in water and methanol, but not in organic solvents such as chloroform or ether. Fmoc-OSu is also a fluorescent derivative that can be used to label glycan structures in primary cells. The reaction solution with anhydrous sodium carbonate and glycan produces a cyclic peptide. This reaction is carried out at room temperature with analytical methods using a spectrophotometer or high performance liquid chromatography (HPLC).Formula:C19H15NO5Purity:Min. 95%Color and Shape:White PowderMolecular weight:337.33 g/molFmoc-ONSU
CAS:Purity:98.0%Color and Shape:Solid, Powder or Crystalline PowderMolecular weight:337.33099365234375Fmoc N-Hydroxysuccinimide Ester
CAS:Stability Moisture Sensitive Applications Used in conjunction with Isothiocyanate to conduct partial Edman Degradation on biologically active peptides. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Heidenreich, O., et al.: J. Biol. Chem., 269, 2131 (1994), Kothe, U., et al.: Anal. Biochem., 356, 148 (2006), Thakkar, A., et al.: Anal. Chem., 78, 5935 (2006),Formula:C19H15NO5Color and Shape:NeatMolecular weight:337.33N-(9H-Fluoren-2-ylmethoxycarbonyloxy)succinimide, 98%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C19H15NO5Purity:98%Color and Shape:White to off-white, PowderMolecular weight:337.33FMOC-OSu extrapure AR, 99%
CAS:Formula:C19H15NO5Purity:min. 99.0%Color and Shape:White to off - white, PowderMolecular weight:337.33N-(9-Fluorenylmethoxycarbonyloxy)succinimide, 98%
CAS:N-(9-Fluorenylmethoxycarbonyloxy)succinimide is the most efficient reagent for the selective preparation of N-(9-fluorenylmethoxycarbonyl) derivatives of hydroxy-amino acids. Dipeptide formation is lower than with the chloroformate, Fmoc-Cl. It is also employed in the synthesis of glycopeptides. 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 Scientific Chemicals.Formula:C19H15NO5Purity:98%Color and Shape:Powder, WhiteMolecular weight:337.33N-[(9H-Fluoren-9-ylmethoxy)carbonyloxy]succinimide
CAS:Formula:C19H15NO5Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:337.33Fmoc-OSu
CAS:Most efficient reagent for the selective preparation of Fmoc-derivatives of hydroxy amino acids in high yield. The advantage of Fmoc-OSu is that little or no oligopeptides are formed when amino acid derivatives are prepared. The use of this reagent in the synthesis of glycopeptides has been reported as well.Formula:C19H15NO5Purity:99.8%Color and Shape:WhiteMolecular weight:337.33Fmoc-OSu
CAS:Fmoc-OSu is a synthetic amino acid that is used in the synthesis of peptides and other biomolecules. It can be synthesized by solid-phase peptide synthesis using Fmoc chemistry, which involves an acid-labile protecting group. Fmoc-OSu has been shown to inhibit cancer cell growth, although its mechanism is not known. Fmoc-OSu has been shown to have anti-inflammatory effects by inhibiting the proinflammatory cytokine TNFα. Fmoc-OSu has also been shown to have glycan binding properties, which may be due to its ability to bind with sialic acid residues on glycoproteins or glycolipids.Formula:C19H15NO5Purity:Min. 98.0 Area-%Molecular weight:337.33 g/molFmoc N-hydroxysuccinimide ester
CAS:Formula:C19H15NO5Purity:≥ 98.0%Color and Shape:White to off-white crystalline powderMolecular weight:337.341-({[(9H-Fluoren-9-yl)methoxy]carbonyl}oxy)pyrrolidine-2,5-dione
CAS:1-({[(9H-Fluoren-9-yl)methoxy]carbonyl}oxy)pyrrolidine-2,5-dioneFormula:C19H15NO5Purity:By hplc: 99.5% by area (Typical Value in Batch COA)Color and Shape: white solidMolecular weight:337.33g/mol
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