206554-92-9

Basic information

• Product Name: tert-butylpiperazine-4-[[(4′-chloromethyl)benzoyl]-1′-carbonyl]-1-carboxylate
• Synonyms: tert-butylpiperazine-4-[[(4′-chloromethyl)benzoyl]-1′-carbonyl]-1-carboxylate
• CAS NO: 206554-92-9
• Molecular Weight: 338.834
• Mol File: 206554-92-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: tert-butylpiperazine-4-[[(4′-chloromethyl)benzoyl]-1′-carbonyl]-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butylpiperazine-4-[[(4′-chloromethyl)benzoyl]-1′-carbonyl]-1-carboxylate(206554-92-9)
• EPA Substance Registry System: tert-butylpiperazine-4-[[(4′-chloromethyl)benzoyl]-1′-carbonyl]-1-carboxylate(206554-92-9)

Safety Data

• Hazardous Substances Data: 206554-92-9(Hazardous Substances Data)

Upstream product

• 876-08-4 p-(chloromethyl)benzoyl chloride 
• 57260-71-6 1-t-Butoxycarbonylpiperazine 
• 861359-74-2 diisopropylethyl amine 

Downstream Products

• 216867-28-6 1-(tert-butoxycarbonyl)-4-[4-(2,6-dimethylpiperidinomethyl)benzoyl]piperazine 
• 216867-08-2 1-(tert-butoxycarbonyl)-4-(4-(N-ethyl-tert-butylaminomethyl)benzoyl)piperazine 

Relevant articles and documents

Solution phase combinatorial chemistry. Discovery of 13- and 15-membered polyazapyridinocyclophane libraries with antibacterial activity

A solution phase simultaneous addition of functionalities (SPSAF) combinatorial approach was utilized to synthesize 40 polyazacyclophane libraries (total complexity of 4275). Eighteen different functionality sets, utilizing 42 functionalities, were design

Benzoate compound as well as preparation method and application thereof

The invention relates to a benzoate compound as well as a preparation method and application thereof. The small-molecule compound is the benzoate compound, namely, (E)-methyl4-((4-(4-(4-(3-methoxy-3-oxoprop-1-en-1-yl)benzoyl)piperazinenzoyl)piperazinenzoy

Substituted cyclic compounds and mixtures comprising same

Novel chemical compounds and mixtures of same are provided having antibacterial and other utilities. The mixtures preferably are formed by reacting a cyclic scaffold moiety with a set of chemical substituients. Libraries formed in accordance with the inve