117833-18-8 | Ac-Asp(OtBu)-OH

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$15.00	$11.00
5g	98%	in stock	$37.00	$26.00
10g	98%	in stock	$72.00	$51.00
25g	98%	in stock	$106.00	$75.00
100g	98%	in stock	$386.00	$270.00

Description

• Catalog Number: AD74876
• Chemical Name: Ac-Asp(OtBu)-OH
• CAS Number: 117833-18-8
• Molecular Formula: C10H17NO5
• Molecular Weight: 231.2457
• MDL Number: MFCD00236746
• SMILES: CC(=O)N[C@H](C(=O)O)CC(=O)OC(C)(C)C

Computed Properties

• Complexity: 292
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 6

Upstream Synthesis Route

(S)-2-Acetamido-4-(tert-butoxy)-4-oxobutanoic acid is a versatile compound used in chemical synthesis for its unique properties and reactivity. This compound serves as a key intermediate in the synthesis of various organic molecules and pharmaceuticals. Its chiral nature, with a specific configuration at the carbon atom, enables precise control over the stereochemistry of the final product.In organic synthesis, (S)-2-Acetamido-4-(tert-butoxy)-4-oxobutanoic acid is commonly employed as a building block for the preparation of complex molecules. Its functional groups can participate in a variety of chemical reactions, such as nucleophilic acyl substitutions, amide bond formations, and asymmetric transformations. This compound is particularly valuable in the synthesis of peptides, where its acetyl and amide functionalities play a crucial role in peptide bond formation.Additionally, the tert-butoxy group in (S)-2-Acetamido-4-(tert-butoxy)-4-oxobutanoic acid acts as a protecting group, shielding specific functionalities during chemical reactions and allowing for selective manipulations. This protection-deprotection strategy is essential in multi-step syntheses to prevent unwanted side reactions and ensure the desired outcome.Overall, (S)-2-Acetamido-4-(tert-butoxy)-4-oxobutanoic acid is a valuable tool in the toolbox of synthetic chemists for the construction of diverse compounds with controlled stereochemistry and functionality. Its applications extend to the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties.