1076197-00-6 | Fmoc-3-amino-2,2-dimethyl-propionic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$139.00	$97.00
250mg	95%	in stock	$211.00	$148.00
1g	95%	in stock	$387.00	$271.00
5g	95%	in stock	$1,412.00	$989.00

Description

• Catalog Number: AI07236
• Chemical Name: Fmoc-3-amino-2,2-dimethyl-propionic acid
• CAS Number: 1076197-00-6
• Molecular Formula: C20H21NO4
• Molecular Weight: 339.38503999999995
• MDL Number: MFCD09952626
• SMILES: O=C(NCC(C(=O)O)(C)C)OCC1c2ccccc2-c2c1cccc2

Upstream Synthesis Route

The compound 3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2,2-dimethylpropanoic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure incorporates a fluorenyl group, a carbamate functionality, and a branched aliphatic side chain, making it valuable for various synthetic applications.One key utility of $name$ in chemical synthesis is as a protecting group for amines. The carbamate group offers protection to the amino functionality, allowing selective modification of other reactive sites in a molecule. This is particularly useful in multi-step organic syntheses where the amine group needs to be preserved until a specific stage.Additionally, the presence of the fluorenyl moiety in $name$ confers steric hindrance and enhanced stability to the compound, making it suitable for use in complex chemical transformations. The bulky fluorenyl group can influence the reactivity and selectivity of reactions, leading to the formation of unique chemical products.Moreover, the 2,2-dimethylpropanoic acid moiety in $name$ provides a chiral center, offering opportunities for asymmetric synthesis. By utilizing $name$ as a chiral building block, enantioselective reactions can be achieved, leading to the production of enantiomerically pure compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.Overall, the strategic incorporation of 3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2,2-dimethylpropanoic acid in chemical synthesis enables the modular construction of diverse molecular architectures with tailored functionalities, demonstrating its significance in advancing synthetic methodologies and expanding the scope of organic chemistry.