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795895

Sigma-Aldrich

2-(2-Boc-5-oxa-2-azaspiro[3.4]octan-7-yl)acetic acid

Sinónimos:

2-(2-(tert-Butoxycarbonyl)-5-oxa-2-azaspiro[3.4]octan-7-yl)acetic acid

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About This Item

Fórmula empírica (notación de Hill):
C13H21NO5
Número de CAS:
1330763-34-2
Peso molecular:
271.31
MDL number:
MFCD20230643
UNSPSC Code:
12352100
PubChem Substance ID:
329768519
NACRES:
NA.22

form

powder

storage temp.

2-8°C

SMILES string

CC(C)(C)OC(N1CC2(CC(CC(O)=O)CO2)C1)=O

InChI

1S/C13H21NO5/c1-12(2,3)19-11(17)14-7-13(8-14)5-9(6-18-13)4-10(15)16/h9H,4-8H2,1-3H3,(H,15,16)

InChI key

LTMIADFDXMGGRP-UHFFFAOYSA-N

General description

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.

Other Notes

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

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

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Artículos

Spirocyclic Building Blocks for Scaffold Assembly

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

Contenido 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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