7145-74-6

Usage

Explanation

The chemical compound is commonly referred to by this name.

Explanation

Another name used for the compound, highlighting the presence of the fluorenylmethyl group and isocyanate functional group.

Explanation

The compound's formula represents the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the molecule.

Explanation

1-isocyanato-9H-fluoren-9-one is derived from the parent compound fluorene, a polycyclic aromatic hydrocarbon.

Explanation

The compound contains an isocyanate group (-NCO), which is responsible for its reactivity and applications in organic synthesis.

Explanation

In peptide synthesis, 1-isocyanato-9H-fluoren-9-one is used to protect amino acids from unwanted side reactions until they are deprotected at a later stage.

Explanation

The compound is a solid, not a liquid or gas.

Explanation

1-isocyanato-9H-fluoren-9-one does not dissolve in water, which can be important for its applications in organic synthesis.

Explanation

The compound dissolves in organic solvents such as acetone and ether, which is useful for its applications in organic synthesis and handling.

Explanation

1-isocyanato-9H-fluoren-9-one is a valuable reagent in organic synthesis due to its ability to protect amino acids and its compatibility with various reaction conditions.

Explanation

The compound is used in the production of peptide-based drugs and biomolecules, making it important for the development of new therapies and technologies.

Explanation

Due to its high reactivity, 1-isocyanato-9H-fluoren-9-one can pose potential health risks and should be handled with caution in laboratory settings.

Upstream product

• 100540-70-3 9-oxo-fluorene-1-carbonyl azide 
• 55341-62-3 9-oxo-9H-fluorene-1-carbonyl chloride