Substance
ID:344571
Names and Identifiers
IUPAC name
2,5-dioxopyrrolidin-1-yl 9H-fluoren-9-ylmethyl carbonate
IUPAC Traditional name
2,5-dioxopyrrolidin-1-yl 9H-fluoren-9-ylmethyl carbonate
Synonyms
9-Fluorenylmethyl N-succinimidyl carbonateN-(9-Fluorenylmethoxycarbonyloxy)succinimideFmoc-OSuFmoc N-hydroxysuccinimide ester9-芴甲基 N-琥珀酰亚胺基碳酸酯9-芴甲基 N-琥珀酰亚氨基碳酸酯N-(9-芴甲氧羰基氧基)琥珀酰亚胺
Registration numbers
CAS Number
EC Number
Beilstein Number
MDL Number
PubChem SID
Properties
Product Information
Empirical Formula (Hill Notation)
C19H15NO5
Purity
≥98.0% (HPLC)
Safety Information
GHS Signal Word
Warning
European Hazard Symbols
Harmful (Xn)
Nature polluting (N)GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
GHS Precautionary statements
P273-P280
GHS Hazard statements
H302-H317-H411
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Risk Statements
22-43-51/53
MSDS Link
German water hazard class
3
Safety Statements
24-37-61
Storage Temperature
2-8°C
Physical Property
Melting Point
150-153 °C(lit.)
Molecule Details
Application
Most efficient reagent for the selective preparation of N-(9-fluorenylmethoxycarbonyl) derivatives of hydroxy-amino acids in high yield. Dipeptide formation is lower than with the chloroformate, Fmoc-Cl. It has been employed in the synthesis of glycopeptides.
Packaging
5, 25, 100 g in glass bottle
Most efficient reagent for the selective preparation of N-(9-fluorenylmethoxycarbonyl) derivatives of hydroxy-amino acids in high yield. Dipeptide formation is lower than with the chloroformate, Fmoc-Cl. It has been employed in the synthesis of glycopeptides.
Packaging
5, 25, 100 g in glass bottle
Molecular Spectra
No Data Available
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References
No Data Available
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