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品質等級
形狀
powder
mp
60-63 °C
應用
peptide synthesis
儲存溫度
15-25°C
InChI
1S/C15H11ClO2/c16-15(17)18-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2
InChI 密鑰
IRXSLJNXXZKURP-UHFFFAOYSA-N
一般說明
(9-Fluorenylmethyl) chloroformate, also known as Fmoc chloride, is a highly versatile reagent with varied applications in organic synthesis. It is most frequently used to introduce the base-labile Fmoc-protecting group to amine functionalities, particularly during the production of Fmoc-protected amino acids. Fmoc-chloride has also been used to generate mixed carboxylic and carbonic anhydrides to facilitate amide and ester bond formation. It is soluble in common organic solvents such as dichloromethane, tetrahydrofuran, and dimethylformamide.
應用
Recent applications of (9-Fluorenylmethyl) chloroformate include:
- (9-Fluorenylmethyl) chloroformate can be used as a coupling reagent.
- In the synthesis of amino acid esters. Fmoc chloride activates the carboxylic acid group of the amino acid, allowing it to react with an alcohol to form the ester.
- In the preparation of lysogangliosides.
- In the solid-phase peptide synthesis of DOPA-containing peptides.
訊號詞
Danger
危險聲明
危險分類
Eye Dam. 1 - Skin Corr. 1B
安全危害
儲存類別代碼
8A - Combustible, corrosive hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
Synthesis of Reactive Amino Acid Esters by Using 9-Fluorenylmethyl Chloroformate
Synfacts, 16, 1247-1247 (2020)
9-Fluorenylmethoxycarbonyl amino-protecting group
The Journal of Organic Chemistry, 37, 3404-3404 (1972)
Synthesis of peptides containing DOPA (3, 4-dihydroxyphenylalanine)
Tetrahedron, 6139-6146 (2001)
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