1086394-57-1 | tert-Butyl 2,6-diazaspiro[3.5]nonane-2-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
50mg	97%	in stock	$70.00	$49.00
100mg	97%	in stock	$126.00	$89.00
250mg	97%	in stock	$212.00	$149.00
500mg	97%	in stock	$300.00	$210.00
1g	97%	in stock	$433.00	$304.00
2.5g	97%	in stock	$1,055.00	$739.00
5g	97%	in stock	$1,516.00	$1,062.00

Description

• Catalog Number: AD65897
• Chemical Name: tert-Butyl 2,6-diazaspiro[3.5]nonane-2-carboxylate
• CAS Number: 1086394-57-1
• Molecular Formula: C12H22N2O2
• Molecular Weight: 226.3153
• MDL Number: MFCD11053736
• SMILES: O=C(N1CC2(C1)CCCNC2)OC(C)(C)C

Upstream Synthesis Route

The tert-Butyl 2,6-diazaspiro[3.5]nonane-2-carboxylate is a versatile compound widely used in chemical synthesis as a building block for the construction of various organic molecules. This unique compound serves as a key intermediate in the synthesis of diverse pharmaceuticals, agrochemicals, and specialty chemicals due to its structural characteristics and reactivity.In chemical synthesis, tert-Butyl 2,6-diazaspiro[3.5]nonane-2-carboxylate plays a crucial role in the formation of complex molecular structures through its ability to undergo a range of transformations. As a spirocyclic compound, it offers a high level of stereochemical control, allowing for the creation of chiral centers and enantiomerically pure products. Additionally, its tert-butyl ester group provides protection for functional groups during synthetic manipulations, enhancing the overall efficiency of the synthesis.Furthermore, the presence of the diazaspiro motif in this compound imparts unique reactivity and functionality, making it a valuable building block for the design and synthesis of bioactive compounds. Its structural features make it particularly suitable for the construction of heterocyclic frameworks and fused ring systems, which are commonly found in drug molecules and natural products.Overall, tert-Butyl 2,6-diazaspiro[3.5]nonane-2-carboxylate serves as a versatile and indispensable tool in the hands of synthetic chemists, enabling them to access a wide array of structurally diverse and biologically relevant compounds through strategic transformations and manipulations.