368866-21-1

Basic information

• Product Name: 1,3-Piperidinedicarboxylicacid,3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,1-(1,1-dimethylethyl)ester(9CI)
• Synonyms: 1,3-Piperidinedicarboxylicacid,3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,1-(1,1-dimethylethyl)ester(9CI);1-Boc-3-FMoc-aMino-3-piperidinecarboxylic acid
• CAS NO: 368866-21-1
• Molecular Formula: C₂₆H₃₀N₂O₆
• Molecular Weight: 466.53
• Product Categories: FMOC
• Mol File: 368866-21-1.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-Piperidinedicarboxylicacid,3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,1-(1,1-dimethylethyl)ester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Piperidinedicarboxylicacid,3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,1-(1,1-dimethylethyl)ester(9CI)(368866-21-1)
• EPA Substance Registry System: 1,3-Piperidinedicarboxylicacid,3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,1-(1,1-dimethylethyl)ester(9CI)(368866-21-1)

Safety Data

• Hazardous Substances Data: 368866-21-1(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 26 carbon (C) atoms, 31 hydrogen (H) atoms, 1 nitrogen (N) atom, and 5 oxygen (O) atoms.

Explanation

This is the commonly used name for the compound, which is derived from its structural features. "Boc" refers to the tert-butyloxycarbonyl group, "N-Fmoc" indicates the presence of a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group on the nitrogen atom, and "L-OH" signifies the presence of a hydroxyl (OH) group on the L-enantiomer of the molecule.

Explanation

The compound is a derivative of 1,3-piperidinedicarboxylic acid, which is a dicarboxylic acid with a piperidine ring. The specific derivative in question has a (9H-fluoren-9-ylmethoxy)carbonyl group attached to the nitrogen atom and a 1,1-dimethylethyl ester group at the 1-position.

Explanation

The compound is used in the synthesis of various pharmaceuticals, particularly peptide-based drugs. Its protecting group properties make it useful for the selective protection of amino acid residues during the synthesis process.

Explanation

As a protecting group, it helps prevent unwanted reactions from occurring at the amino acid's functional groups during peptide synthesis. This allows for the controlled formation of peptide bonds and the synthesis of complex peptide structures.

Explanation

The compound serves as a building block for the creation of complex organic molecules in the field of organic chemistry. Its unique structure and functional groups make it a versatile starting material for the synthesis of various organic compounds.

Explanation

The compound exists as an L-enantiomer, which means it has a specific three-dimensional arrangement of atoms that is non-superimposable with its mirror image (D-enantiomer). This chirality is important for its biological activity and applications in pharmaceuticals and organic synthesis.

Structure

1,3-Piperidinedicarboxylic acid derivative

Application

Pharmaceutical synthesis

Application

Protecting group for amino acids

Application

Organic chemistry building block

Chirality

L-enantiomer

Downstream Products

• 368866-17-5 3-amino-1-(tert-butoxycarbonyl)piperidine-3-carboxylic acid