181518-87-6 | Butanoic acid, 4-(dimethylamino)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2S)-

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$355.00	$248.00
250mg	95%	in stock	$497.00	$348.00
500mg	95%	in stock	$720.00	$504.00
1g	95%	in stock	$943.00	$660.00

Description

• Catalog Number: AA96925
• Chemical Name: Butanoic acid, 4-(dimethylamino)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2S)-
• CAS Number: 181518-87-6
• Molecular Formula: C11H22N2O4
• Molecular Weight: 246.3034
• MDL Number: MFCD24465582
• SMILES: CN(CC[C@@H](C(=O)O)NC(=O)OC(C)(C)C)C

Computed Properties

• Complexity: 271
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 7
• XLogP3: -1.3

Upstream Synthesis Route

(S)-2-(tert-Butoxycarbonylamino)-4-(dimethylamino)butanoic acid, also known as Boc-Dma-OH, is a valuable compound widely used in chemical synthesis. This chiral amino acid derivative plays a crucial role in the creation of asymmetrical structures and the synthesis of pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, Boc-Dma-OH serves as a versatile building block due to its unique properties. It acts as a key intermediate in the preparation of peptides, which are essential in drug development and biological research. By incorporating this compound into peptide synthesis, chemists can control the stereochemistry of the final product, enabling the production of specific enantiomers with enhanced biological activity.Furthermore, Boc-Dma-OH is instrumental in the creation of complex molecules through its compatibility with a variety of coupling reactions, such as amide bond formation and peptide coupling. Its tert-butoxycarbonyl (Boc) protecting group provides stability during synthesis, allowing for selective deprotection at a later stage. This protective group strategy facilitates the construction of intricate molecular architectures with high efficiency and precision.Overall, the application of (S)-2-(tert-Butoxycarbonylamino)-4-(dimethylamino)butanoic acid in chemical synthesis offers a versatile and effective approach to the synthesis of biologically active compounds and structurally diverse molecules. Its utility in peptide synthesis and functional group manipulation makes it a valuable tool for chemists striving to advance the frontier of organic chemistry and drug discovery.