1204820-62-1 | Ethyl 3-boc-3-azabicyclo[3.1.0]hexane-1-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$88.00	$62.00
500mg	95%	in stock	$132.00	$93.00
1g	95%	in stock	$226.00	$159.00

Description

• Catalog Number: AE47074
• Chemical Name: Ethyl 3-boc-3-azabicyclo[3.1.0]hexane-1-carboxylate
• CAS Number: 1204820-62-1
• Molecular Formula: C13H21NO4
• Molecular Weight: 255.3101
• MDL Number: MFCD19443438
• SMILES: CCOC(=O)C12CN(CC2C1)C(=O)OC(C)(C)C

Computed Properties

• Complexity: 374
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Undefined Atom Stereocenter Count: 2
• XLogP3: 1.3

Upstream Synthesis Route

3-tert-Butyl 1-ethyl 3-azabicyclo[3.1.0]hexane-1,3-dicarboxylate, also known as $name$, is a versatile compound widely used in chemical synthesis. With its unique structure and functional groups, this compound serves as an important building block in the creation of various organic molecules. In chemical synthesis, $name$ plays a crucial role in the formation of complex molecular structures due to its ability to undergo different types of reactions. Its tert-butyl and ethyl groups provide steric hindrance and enhance the compound's stability, making it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and fine chemicals.One key application of $name$ in chemical synthesis is as a starting material for the synthesis of heterocyclic compounds. By reacting $name$ with various reagents and catalysts, chemists can access a wide range of fused heterocycles, which are important structural motifs found in many biologically active molecules. Additionally, the presence of the azabicyclo[3.1.0]hexane core in $name$ imparts unique stereochemical properties to the resulting products, making it a versatile tool for stereocontrolled synthesis.Furthermore, the 1,3-dicarboxylate moiety in $name$ enables it to participate in a variety of cross-coupling reactions, leading to the formation of C-C and C-heteroatom bonds. This feature is particularly valuable in the synthesis of complex organic molecules, where the ability to selectively introduce functional groups in a controlled manner is essential.Overall, the strategic incorporation of $name$ in chemical synthesis offers synthetic chemists a powerful means to access diverse molecular architectures with tailored properties, making it a valuable component in the toolkit of modern organic synthesis.