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802263

Sigma-Aldrich

tert-Butyl 8-hydroxy-5-thia-2-azaspiro[3.4]octane-2-carboxylate 5,5-dioxide

≥95%

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About This Item

Fórmula empírica (Notação de Hill):
C11H19NO5S
Número CAS:
1340481-90-4
Peso molecular:
277.34
Número MDL:
MFCD22370061
Código UNSPSC:
12352100
ID de substância PubChem:
329768734
NACRES:
NA.22

Ensaio

≥95%

forma

powder

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

OC(CCS1(=O)=O)C21CN(C(OC(C)(C)C)=O)C2

InChI

1S/C11H19NO5S/c1-10(2,3)17-9(14)12-6-11(7-12)8(13)4-5-18(11,15)16/h8,13H,4-7H2,1-3H3

chave InChI

OJYOLQAIQYHQOC-UHFFFAOYSA-N

Aplicação

Spirocyclic building block was first synthesized by Carreira and coworkers, which provides a new area of chemical space with straightforward functional handles for further diversification.

Outras notas

Synthesis of Novel Azaspiro[3.4]octanes as Multifunctional Modules in Drug Discovery

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Artigos

Spirocyclic Building Blocks for Scaffold Assembly

Spirocyclic modules containing four-membered rings are currently of growing interest to discovery chemists.

Conteúdo relacionado

Carreira Group – Professor Product Portal

The Carreira Research Group is focused on expanding and creating access to uncharted landscape in chemical space. In joint efforts with SpiroChem, Carreira develops innovative spirocyclic building blocks, seeking to make them available to the community at large. Molecules constructed from these building blocks take on unique three-dimensional profiles due to the underlying spirocyclic scaffold, enriched by the presence of diverse combinations of exit vectors as sites for functionalization. Importantly, the spirocyclic building blocks possess physicochemical properties useful in the drug discovery process. Thus, drug leads can be tuned through appending these subunits to the periphery of a given scaffold. Moreover, these compact modules represent a useful collection of unprecedented inputs for fragment-based libraries. In all applications, the inherent novelty of the structure affords researchers new opportunities to run wild in their designs and avenues to chemical space – with their imagination as the sole limitations. We are proud to partner in the efforts to make these building blocks widely available.

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