111662-64-7 | Fmoc-gla(otbu)2-oh

Packsize	Purity	Availability	Price	Discounted Price
50mg	95%	in stock	$99.00	$69.00
100mg	95%	in stock	$193.00	$136.00
250mg	>95%	in stock	$358.00	$250.00
1g	>95%	in stock	$928.00	$649.00
5g	>95%	in stock	$4,215.00	$2,950.00

Description

• Catalog Number: AD75628
• Chemical Name: Fmoc-gla(otbu)2-oh
• CAS Number: 111662-64-7
• Molecular Formula: C29H35NO8
• Molecular Weight: 525.5901
• MDL Number: MFCD00038770
• SMILES: O=C(N[C@H](C(=O)O)CC(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)OCC1c2ccccc2c2c1cccc2

Computed Properties

• Complexity: 823
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 38
• Hydrogen Bond Acceptor Count: 8
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 13
• XLogP3: 5

Upstream Synthesis Route

The (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-4-(tert-butoxycarbonyl)-5-oxopentanoic acid, also known as $name$, is a versatile compound widely used in chemical synthesis processes. Its primary application lies in the field of peptide synthesis, where it serves as a key building block for creating complex peptides. $name$ plays a crucial role in peptide chemistry by acting as a protecting group for amino acids during synthesis. The tert-butoxycarbonyl (Boc) and fluorenylmethoxycarbonyl (Fmoc) groups present in $name$ are specifically designed to shield reactive functional groups within the peptide chain, allowing for selective and controlled reactions at targeted sites. Moreover, $name$ facilitates the assembly of peptides with high purity and efficiency, ensuring the accurate sequence of amino acids in the final product. Its unique structure and properties make it a valuable tool for chemists and researchers involved in the development of novel peptides for various applications in biotechnology, pharmaceuticals, and materials science.