1093198-33-4 | (R)-Methyl 2-amino-3-(tert-butoxycarbonylamino)-3-methylbutanoate

Packsize	Purity	Availability	Price	Discounted Price
1mg	95	2 weeks	$105.00	$73.00
2mg	95	2 weeks	$123.00	$86.00
3mg	95	2 weeks	$149.00	$105.00
5mg	95	2 weeks	$168.00	$118.00
10mg	95	2 weeks	$193.00	$135.00
100mg	95%	2 weeks	$603.00	$422.00
250mg	95%	2 weeks	$1,002.00	$701.00
500mg	95%	2 weeks	$1,345.00	$942.00
1g	95%	2 weeks	$1,860.00	$1,302.00
2g	95%	2 weeks	$3,362.00	$2,353.00

Description

• Catalog Number: AI07764
• Chemical Name: (R)-Methyl 2-amino-3-(tert-butoxycarbonylamino)-3-methylbutanoate
• CAS Number: 1093198-33-4
• Molecular Formula: C11H22N2O4
• Molecular Weight: 246.3034
• MDL Number: MFCD28991774
• SMILES: COC(=O)[C@@H](C(NC(=O)OC(C)(C)C)(C)C)N

Computed Properties

• Complexity: 294
• 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: 6
• XLogP3: 0.6

Upstream Synthesis Route

In chemical synthesis, (R)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)-3-methylbutanoate is a valuable building block for the creation of complex molecules, particularly in the field of medicinal chemistry. This compound, known for its chirality and stability, plays a crucial role as a key intermediate in the development of pharmaceuticals and bioactive compounds.By incorporating (R)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)-3-methylbutanoate into synthetic pathways, chemists can introduce specific functional groups and stereochemical elements with precision. Its unique structure allows for selective manipulation, leading to the formation of structurally diverse molecules with desired properties. This compound serves as a versatile tool for the construction of peptide sequences, amino acid derivatives, and other biologically relevant scaffolds.Furthermore, the presence of the tert-butoxycarbonyl protecting group enhances the stability and reactivity of (R)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)-3-methylbutanoate during various synthetic transformations. This protection strategy enables controlled reactions and sequential modifications, facilitating the synthesis of intricate molecular architectures.Overall, (R)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)-3-methylbutanoate serves as a versatile tool in chemical synthesis, enabling the efficient construction of complex molecules with tailored structures and functionalities. Its application in medicinal chemistry and drug discovery highlights its significance as a key component in the development of novel therapeutics and biologically active compounds.