1211586-14-9 | tert-Butyl octahydro-1h-pyrrolo[3,2-b]pyridine-1-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
50mg	96%	in stock	$128.00	$90.00
100mg	96%	in stock	$166.00	$117.00
250mg	96%	in stock	$246.00	$173.00
1g	96%	in stock	$645.00	$452.00

Description

• Catalog Number: AE42523
• Chemical Name: tert-Butyl octahydro-1h-pyrrolo[3,2-b]pyridine-1-carboxylate
• CAS Number: 1211586-14-9
• Molecular Formula: C12H22N2O2
• Molecular Weight: 226.31528000000012
• MDL Number: MFCD18382710
• SMILES: O=C(N1CCC2C1CCCN2)OC(C)(C)C

Computed Properties

• Complexity: 273
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• Undefined Atom Stereocenter Count: 2
• XLogP3: 1.4

Upstream Synthesis Route

The tert-Butyl octahydro-1H-pyrrolo[3,2-b]pyridine-1-carboxylate serves as a valuable intermediate in chemical synthesis due to its versatile reactivity and structural features. This compound plays a crucial role in the construction of complex organic molecules through various synthetic routes. In particular, it can be employed as a key building block for the preparation of pharmacologically active compounds, agrochemicals, and materials with specific properties.One of the significant applications of tert-Butyl octahydro-1H-pyrrolo[3,2-b]pyridine-1-carboxylate lies in its ability to participate in diverse transformations such as functional group manipulations, ring-closure reactions, and stereospecific transformations. This compound's structural motif enables the introduction of substituents at multiple positions, facilitating the synthesis of structurally diverse molecules with tailored properties.Furthermore, tert-Butyl octahydro-1H-pyrrolo[3,2-b]pyridine-1-carboxylate can be utilized in asymmetric synthesis strategies to access enantiomerically pure compounds. Its chiral nature allows for the creation of stereochemically complex molecules with high levels of selectivity and efficiency, making it a valuable tool in the hands of synthetic chemists striving to access complex molecular architectures.