CAS 116747-54-7

Fmoc-Ala-Gly-OH

Description:

Fmoc-Ala-Gly-OH, also known as Fmoc-Alanine-Glycine-OH, is a protected dipeptide that consists of the amino acids alanine and glycine. The "Fmoc" (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality of alanine, allowing for selective reactions during peptide synthesis. This compound is typically used in solid-phase peptide synthesis due to its stability and ease of removal of the Fmoc group under mild basic conditions. Fmoc-Ala-Gly-OH is characterized by its relatively low solubility in non-polar solvents and moderate solubility in polar solvents, making it suitable for various biochemical applications. The presence of both hydrophobic (alanine) and hydrophilic (glycine) residues contributes to its potential interactions in biological systems. Additionally, this dipeptide can serve as a building block for more complex peptides and proteins, facilitating studies in peptide chemistry and biochemistry. Its CAS number, 116747-54-7, uniquely identifies this compound in chemical databases, aiding in research and application.

Formula: C₂₀H₂₀N₂O₅

Fmoc-Ala-Gly-OH

CAS: 116747-54-7

Bachem ID: 4012679.

Formula: C₂₀H₂₀N₂O₅

Purity: 99.3%

Color and Shape: White Powder

Molecular weight: 368.39

Ref: 01-4012679

Glycine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanyl-

CAS: 116747-54-7

Formula: C₂₀H₂₀N₂O₅

Purity: 98%

Color and Shape: Solid

Molecular weight: 368.3832

Ref: IN-DA000D63

Fmoc-Ala-Gly-OH

CAS: 116747-54-7

Fmoc-Ala-Gly-OH

Purity: 95%

Molecular weight: 368.38g/mol

Ref: 54-OR36469

Fmoc-Ala-Gly-OH

CAS: 116747-54-7

Fmoc-Ala-Gly-OH is a building block for peptide synthesis and Fmoc protected l-amino acid. It is an amino acid that belongs to the group of Fmoc protected l-amino acids. This amino acid can be used as a building block for peptide synthesis, which is a technique for the chemical synthesis of peptides. The general method involves the activation of carboxyl groups on one end of the growing peptide chain with an activating agent such as dicyclohexylcarbodiimide or diisopropylcarbodiimide. The activated carboxyl group reacts with an amine (or ammonia) to form an amide bond, linking the new molecule to the preceding one in the chain. This reaction produces a molecule with a free carboxyl group at one end, which can then repeat the process.

Formula: C₂₀H₂₀N₂O₅

Purity: Min. 95%

Molecular weight: 368.39 g/mol

Ref: 3D-FAG-1929-PI

Fmoc-L-Ala-Gly-OH

CAS: 116747-54-7

Purity: 98%

Molecular weight: 368.39

Ref: 10-F773736

N-[N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-alanyl]-glycine

Controlled Product

CAS: 116747-54-7

Applications FMOC-ALA-GLY-OH (cas# 116747-54-7) is a useful research chemical.

Formula: C₂₀H₂₀N₂O₅

Color and Shape: Neat

Molecular weight: 368.383

Ref: TR-F657780

Fmoc-Ala-Gly-OH

CAS: 116747-54-7

Fmoc-Ala-Gly-OH is a cell-surface residue that is found on proteins. It is the ligand for a number of protein receptors and has been shown to be involved in factors such as orientation, verotoxin, and neoglycopeptides. Fmoc-Ala-Gly-OH also acts as an inhibitor by binding to glycine and trisaccharide residues. This residue is located at the N-terminal of the protein.

Formula: C₂₀H₂₀N₂O₅

Purity: Min. 95%

Molecular weight: 368.38 g/mol

Ref: 3D-FF111301