106247-35-2 | H-Beta-tBu-DL-Ala-OH

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$42.00	$30.00
1g	98%	in stock	$122.00	$86.00
5g	98%	in stock	$511.00	$358.00
25g	98%	in stock	$2,314.00	$1,620.00

Description

• Catalog Number: AE12634
• Chemical Name: H-Beta-tBu-DL-Ala-OH
• CAS Number: 106247-35-2
• Molecular Formula: C10H13NO4
• Molecular Weight: 211.2145
• MDL Number: MFCD00066078
• SMILES: COc1ccc(c(c1)C(C(=O)O)N)OC
• NSC Number: 522507

Computed Properties

• Complexity: 126
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: -1.3

Upstream Synthesis Route

2-Amino-4,4-dimethylpentanoic acid, also known by its systematic name N-(2,2-dimethylpropyl)-2-aminopentanoic acid, is a versatile compound widely utilized in the field of chemical synthesis. This unique amino acid derivative plays a crucial role as a building block in the preparation of various pharmaceuticals and fine chemicals. Due to its structural features, 2-Amino-4,4-dimethylpentanoic acid can be selectively functionalized and incorporated into complex molecular structures with high efficiency.In chemical synthesis, 2-Amino-4,4-dimethylpentanoic acid serves as a key intermediate for the synthesis of diverse biologically active compounds. Its amino and carboxylic acid functional groups allow for facile derivatization and modification, enabling the creation of custom-designed molecules with specific properties. This compound is particularly valuable in the production of pharmaceuticals targeting various biological pathways and disease states.Moreover, the unique steric and electronic properties of 2-Amino-4,4-dimethylpentanoic acid make it a valuable tool in the asymmetric synthesis of chiral molecules. By incorporating this amino acid derivative into the molecular structure, chemists can introduce chirality with high enantioselectivity, crucial for the development of enantiopure drugs and agrochemicals.Overall, the application of 2-Amino-4,4-dimethylpentanoic acid in chemical synthesis extends beyond its role as a mere building block, showcasing its significance in the creation of complex molecules with tailored functionalities and diverse applications.

Literature

• Potent inhibitors of LXXLL-based protein-protein interactions.

  Chembiochem : a European journal of chemical biology 20051101