269078-72-0 | Fmoc-d-homocyclohexylalanine

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$11.00	$8.00
1g	97%	in stock	$21.00	$15.00
5g	98%	in stock	$82.00	$58.00
10g	98%	in stock	$153.00	$107.00
25g	98%	in stock	$336.00	$235.00
100g	98%	in stock	$1,283.00	$898.00

Description

• Catalog Number: AF62422
• Chemical Name: Fmoc-d-homocyclohexylalanine
• CAS Number: 269078-72-0
• Molecular Formula: C25H29NO4
• Molecular Weight: 407.5021
• MDL Number: MFCD02179644
• SMILES: O=C(N[C@@H](C(=O)O)CCC1CCCCC1)OCC1c2ccccc2c2c1cccc2

Computed Properties

• Complexity: 566
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 30
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 8
• XLogP3: 6.1

Upstream Synthesis Route

The compound (αR)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclohexanebutanoic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure contains a cyclohexanebutanoic acid core with an amino acid-derived fluorenylmethoxy carbonyl protecting group, making it a valuable intermediate in organic chemistry.$name$ is commonly used as a chiral auxiliary in asymmetric synthesis reactions. By selectively controlling the stereochemistry of the compound during a reaction, chemists can efficiently produce enantiomerically pure products. This capability is particularly important in drug discovery and the manufacturing of pharmaceuticals, where the stereochemistry of a molecule can significantly influence its biological activity.In addition, $name$ can also serve as a key component in peptide synthesis. The fluorenylmethoxy carbonyl protecting group helps protect the amine functionality of the amino acid, allowing for controlled deprotection steps and facilitating the sequential assembly of peptides in a defined order.Overall, the application of (αR)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclohexanebutanoic acid in chemical synthesis enables chemists to efficiently access complex molecules with high stereochemical purity, making it an indispensable tool in the field of organic chemistry.