182067-63-6

Basic information

• Product Name: 2,5-Piperazinedione,1,3,4-trimethyl-(9CI)
• Synonyms: 2,5-Piperazinedione,1,3,4-trimethyl-(9CI);1,3,4-TRIMETHYLPIPERAZINE-2,5-DIONE
• CAS NO: 182067-63-6
• Molecular Formula: C7H12N2O2
• Molecular Weight: 0
• Product Categories: PIPERIDINE
• Mol File: 182067-63-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-Piperazinedione,1,3,4-trimethyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Piperazinedione,1,3,4-trimethyl-(9CI)(182067-63-6)
• EPA Substance Registry System: 2,5-Piperazinedione,1,3,4-trimethyl-(9CI)(182067-63-6)

Safety Data

• Hazardous Substances Data: 182067-63-6(Hazardous Substances Data)

Usage

Structure

Cyclic derivative of piperazine with three methyl groups attached to the nitrogen atoms

Physical properties

White crystalline solid, molecular weight of 156.18 g/mol

Uses

Primarily used as an intermediate in the synthesis of pharmaceutical drugs

Industry applications

Potential applications in the pharmaceutical and chemical industries due to its versatile reactivity and structural properties

Biological activity

May possess some biological activity and could be of interest in medicinal chemistry research

Upstream product

• 108584-33-4 N-(2-bromo-propionyl)-N-methyl-glycine 
• 74-89-5 methylamine 
• 4526-77-6 3-methylpiperazine-2,5-dione 
• 74-88-4 methyl iodide 
• 519141-03-8 1-methyl-3-benzyloxycarbonylpiperazine-2,5-dione 
• 519141-04-9 3-benzyloxycarbonyl-1,4-dimethylpiperazine-2,5-dione 
• 519141-10-7 3-benzyloxycarbonyl-1,3-dimethylpiperazine-2,5-dione 
• 519141-14-1 3-benzyloxycarbonyl-1,3,4-trimethylpiperazine-2,5-dione 
• 865879-17-0 benzyl N-[N-t-butoxycarbonylsarcosyl]-2-benzyloxycarbonylglycinate 

Relevant articles and documents

EPIDITHIODIOXOPIPERAZINE COMPOUND OR ITS DERIVATIVES, AND THE USE THEREOF

The present invention relates to an epidithiodioxopiperazine derivative represented by the Chemical Formula 1 or its reduced derivative; a method for preparing a compound represented by Chemical Formula 1 having improved intracellular permeability and mim

Selectivity in radical reactions of alanylglycine anhydride derivatives

Functionalization of N,N′-disubstituted alanylglycine anhydrides under radical conditions is described. The radical (7), generated (i) from reactions of N,N′-disubstituted alanylglycine anhydrides with N-bromosuccinimide, and (ii) from related bromo compounds by reaction with tributyltin deuteride, undergoes carbon-bromine and carbon-deuterium bond formation with moderate to high diastereoselectivities depending on the N-substituents present.