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Key Documents

934410

Sigma-Aldrich

Carbamic acid, N-[2-(1-piperazinyl)ethyl]-, 1,1-dimethylethyl ester

≥95%

Synonym(s):

1,1-Dimethylethyl N-[2-(1-piperazinyl)ethyl]carbamate, 1-(2-((tert-Butoxycarbonyl)amino)ethyl)piperazine, tert-Butyl N-(2-(piperazin-1-yl)ethyl)carbamate, tert-Butyl [2-(piperazin-1-yl)ethyl]carbamate, Carbamic acid, [2-(1-piperazinyl)ethyl]-, 1,1-dimethylethyl ester

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About This Item

Empirical Formula (Hill Notation):
C11H23N3O2
CAS Number:
Molecular Weight:
229.32
MDL number:
UNSPSC Code:
12352108

Quality Level

Assay

≥95%

form

powder

storage temp.

2-8°C

Application

A functionalized cereblon ligand for development of Thalidomide based PROTACs. Allows rapid conjugation with carboxyl linkers due to presence of amine group via peptide coupling reactions. Amenable for linker attachement via reductive amination, and a basic building block for making protein degrader library.

Technology Spotlight:

Degrader Building Blocks for Targeted Protein Degradation

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Legal Information

PROTAC® is a registered trademark of Arvinas Operations, Inc., and is used under license.
PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Daniel P Bondeson et al.
Annual review of pharmacology and toxicology, 57, 107-123 (2016-10-13)
Protein homeostasis networks are highly regulated systems responsible for maintaining the health and productivity of cells. Whereas therapeutics have been developed to disrupt protein homeostasis, more recently identified techniques have been used to repurpose homeostatic networks to effect degradation of

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