741287-48-9

Basic information

• Product Name: tert-butyl 4-(2-methoxyethyl)piperazine-1-carboxylate
• Synonyms: tert-butyl 4-(2-methoxyethyl)piperazine-1-carboxylate
• CAS NO: 741287-48-9
• Molecular Weight: 244.334
• Mol File: 741287-48-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 304.8±32.0 °C(Predicted)
• Density: 1.034±0.06 g/cm3(Predicted)
• CAS DataBase Reference: tert-butyl 4-(2-methoxyethyl)piperazine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 4-(2-methoxyethyl)piperazine-1-carboxylate(741287-48-9)
• EPA Substance Registry System: tert-butyl 4-(2-methoxyethyl)piperazine-1-carboxylate(741287-48-9)

Safety Data

• Hazardous Substances Data: 741287-48-9(Hazardous Substances Data)

Upstream product

• 103-76-4 1-(2-hydroxyethyl)piperazine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 77279-24-4 tert-butyl 4-(2-hydroxyethyl)piperazine-1-carboxylate 
• 74-88-4 methyl iodide 
• 57260-71-6 1-t-Butoxycarbonylpiperazine 
• 6482-24-2 2-Bromoethyl methyl ether 
• 627-42-9 2-chloroethyl methyl ether 

Downstream Products

• 13484-40-7 1-(2-methoxyethyl)piperazine 
• 688763-69-1 6-amino-3-chloro-2-[4-(2-methoxyethyl)-piperazine-1-sulfonyl]-phenol 
• 550370-70-2 1-(2-methoxyethyl)piperazine hydrochloride 

Relevant articles and documents

TARGETING DNA REPAIR IN TUMOR CELLS VIA INHIBITION OF ERCC1-XPF

The current application relates to pyronaridine or 6-chloro-2-methoxyacridine analogs having binding affinity for the ERCC1-XPF hetero-dimerization interface. The compounds can be used for targeting DNA repair in tumor cells via ERCC1-XPF inhibition, ther

THIAZOLE AND OXAZOLE KINASE INHIBITORS

The present invention is concerned with substituted azole derivatives that selectively modulate, regulate, and/or inhibit signal transduction mediated by certain native and/or mutant proteine kinases implicated in a variety of human and animal diseases such as cell proliferative, metabolic, allergic, and degenerative disorders. In particular, several of these compounds are potent and selective Flt-3 inhibitors or/and syk inhibitors.

Discovery and biological evaluation of adamantyl amide 11β-HSD1 inhibitors

A series of adamantyl amide 11β-HSD1 inhibitors has been discovered and chemically modified. Selected compounds are selective for 11β-HSD1 over 11β-HSD2 and possess excellent cellular potency in human and murine 11β-HSD1 assays. Good pharmacodynamic characteristics are observed in ex vivo assays.