29022-11-5 | Fmoc-Gly-OH

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$5.00	$4.00
10g	98%	in stock	$8.00	$5.00
25g	98%	in stock	$9.00	$7.00
100g	98%	in stock	$27.00	$19.00
500g	98%	in stock	$132.00	$92.00
1000g	98%	in stock	$225.00	$157.00

Description

• Catalog Number: AB33605
• Chemical Name: Fmoc-Gly-OH
• CAS Number: 29022-11-5
• Molecular Formula: C17H15NO4
• Molecular Weight: 297.3053
• MDL Number: MFCD00037140
• SMILES: OC(=O)CNC(=O)OCC1c2ccccc2-c2c1cccc2
• NSC Number: 334288

Computed Properties

• Complexity: 403
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 2.7

Upstream Synthesis Route

N-(9-Fluorenylmethoxycarbonyl)glycine is a versatile compound widely utilized in chemical synthesis as a key building block in peptide chemistry. This compound plays a crucial role in the protection and deprotection of amino acids during peptide synthesis. Its Fmoc (9-fluorenylmethoxycarbonyl) group acts as a temporary shielding group for the amino group, allowing for selective reactions to take place at specific sites within a peptide chain.In solid-phase peptide synthesis, N-(9-Fluorenylmethoxycarbonyl)glycine is commonly employed as an Fmoc-protected amino acid derivative. By coupling this compound with other amino acids in a stepwise manner, intricate peptide chains can be efficiently constructed. The Fmoc group can then be easily removed under mild conditions, revealing the free amino group for subsequent coupling reactions.Furthermore, N-(9-Fluorenylmethoxycarbonyl)glycine enables the synthesis of peptides with diverse sequences and functionalities, making it invaluable in the research and production of peptides for various applications, such as drug development, biochemical studies, and materials science. Its compatibility with automated peptide synthesizers further enhances the efficiency and precision of peptide assembly processes.