Fmoc-DL-Nle-OH, with the CAS number 144701-20-2, is a chemical compound commonly used in peptide synthesis. It is a derivative of the amino acid norleucine (Nle) and features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis to protect the amino group during the coupling reactions. The Fmoc group is known for its stability under basic conditions and can be removed under mild acidic conditions, allowing for selective deprotection. This compound is typically a white to off-white solid and is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. Its structure includes both hydrophobic and polar characteristics, making it suitable for various biochemical applications. Fmoc-DL-Nle-OH is particularly valuable in the synthesis of peptides that require specific modifications or in the development of peptide-based drugs. Proper handling and storage are essential due to its potential reactivity and the need for maintaining its integrity during synthesis processes.

Fmoc-DL-Nle-OH

144701-20-2: Fmoc-DL-Nle-OH, with the CAS number 144701-20-2, is a chemical compound commonly used in peptide synthesis. It is a derivative of the amino acid norleucine (Nle) and features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis to protect the amino group during the coupling reactions. The Fmoc group is known for its stability under basic conditions and can be removed under mild acidic conditions, allowing for selective deprotection. This compound is typically a white to off-white solid and is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. Its structure includes both hydrophobic and polar characteristics, making it suitable for various biochemical applications. Fmoc-DL-Nle-OH is particularly valuable in the synthesis of peptides that require specific modifications or in the development of peptide-based drugs. Proper handling and storage are essential due to its potential reactivity and the need for maintaining its integrity during synthesis processes.

CAS 144701-20-2

Fmoc-DL-Nle-OH

FMOC-DL-NLE-OH

Ref: IN-DA00AOTL

2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hexanoic acid

Ref: 54-OR75883

Fmoc-DL-norleucine

Ref: 10-F492873