6-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanehydrazide

≥95%

Reagent Code: #167657
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CAS Number 81186-33-6

science Other reagents with same CAS 81186-33-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.24 g/mol
Formula C₁₀H₁₅N₃O₃
badge Registry Numbers
MDL Number MFCD05865037
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing bioactive molecules, particularly in the development of proteolysis-targeting chimeras (PROTACs). Its structure allows for conjugation between E3 ligase ligands and target protein binders, facilitating targeted protein degradation. Also employed in the preparation of peptide-like polymers and functionalized hydrazides for biochemical assays. Shows potential in creating novel anti-cancer and anti-inflammatory agents due to its ability to form stable linkages in complex molecular architectures.

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inventory 1g
10-20 days ฿39,350.00

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6-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanehydrazide
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Used in pharmaceutical research as an intermediate for synthesizing bioactive molecules, particularly in the development of proteolysis-targeting chimeras (PROTACs). Its structure allows for conjugation between E3 ligase ligands and target protein binders, facilitating targeted protein degradation. Also employed in the preparation of peptide-like polymers and functionalized hydrazides for biochemical assays. Shows potential in creating novel anti-cancer and anti-inflammatory agents due to its ability to

Used in pharmaceutical research as an intermediate for synthesizing bioactive molecules, particularly in the development of proteolysis-targeting chimeras (PROTACs). Its structure allows for conjugation between E3 ligase ligands and target protein binders, facilitating targeted protein degradation. Also employed in the preparation of peptide-like polymers and functionalized hydrazides for biochemical assays. Shows potential in creating novel anti-cancer and anti-inflammatory agents due to its ability to form stable linkages in complex molecular architectures.

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