Fluorenylmethyloxycarbonyl chloride (Fmoc-Cl) is a chloroformate ester. It is used to introduce the fluorenylmethyloxycarbonyl protecting group as the Fmoc carbamate.

The fluorenylmethoxycarbonyl protecting group (Fmoc) is a base -labile amine protecting group used in organic synthesis, particularly in peptide synthesis [1].

Aldrich-160512; Fmoc chloride 0.97; CAS No.: 28920-43-6; Synonyms: 9-Fluorenylmethoxycarbonyl chloride; 9-Fluorenylmethyl chloroformate; Fmoc-Cl; Linear Formula: C15H11ClO2; Empirical Formula: C15H11ClO2; find related products, papers, technical documents, MSDS & more at Sigma-Aldrich.

2021年4月26日 · The reagent the researchers chose to install the Fmoc group was 9-fluorenylmethyloxycarbonyl chloride (Fmoc-Cl), also frequently called 9-fluorenylmethyl chloroformate. They prepared Fmoc-Cl by treating 9-fluorenylmethanol with phosgene (COCl 2).

2021年5月7日 · 9-fluorenylmethyloxycarbonyl (Fmoc) chloride | C30H21ClO4 | CID 56986206 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Synonyms: fluorenylmethyloxycarbonyl chloride Molecular Weight (g/mol): 258.7 Molecular Formula: C15H11ClO2

Fluorenylmethyloxycarbonyl chloride (Fmoc-Cl) is a chloroformate ester. It is used to introduce the fluorenylmethyloxycarbonyl protecting group as the Fmoc carbamate.

Fmoc chloride may be used as derivatizing reagent in pre-column derivatization of the biogenic amines, resolved using HPLC technique.

Fmoc chloride. Synonyms: 9-Fluorenylmethoxycarbonyl chloride, 9-Fluorenylmethyl chloroformate, Fmoc-Cl. CAS 28920-43-6. Molecular Weight 258.70. Browse Fmoc chloride and related products at MilliporeSigma.

2024年8月28日 · The chemical structure of Fmoc-Chloride is based on the fluorenylmethyloxycarbonyl (Fmoc) group, which is attached to a chloride. The fluorenyl group contributes to the stability and reactivity of the molecule, while the chloride atom is crucial for the formation of the reactive intermediate that allows for the efficient protection of amino groups.