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143411-86-3

2,5-Piperazinedione,1-(2-hydroxyethyl)-3,3-dimethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143411-86-3 Structure

  • Basic information

    1. Product Name: 2,5-Piperazinedione,1-(2-hydroxyethyl)-3,3-dimethyl-(9CI)
    2. Synonyms: 2,5-Piperazinedione,1-(2-hydroxyethyl)-3,3-dimethyl-(9CI);1-(2-HYDROXYETHYL)-3,3-DIMETHYLPIPERAZINE-2,5-DIONE
    3. CAS NO:143411-86-3
    4. Molecular Formula: C8 H14 N2 O3
    5. Molecular Weight: 186.21
    6. EINECS: N/A
    7. Product Categories: PIPERIDINE
    8. Mol File: 143411-86-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 458.4±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.163±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 13.74±0.40(Predicted)
    10. CAS DataBase Reference: 2,5-Piperazinedione,1-(2-hydroxyethyl)-3,3-dimethyl-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,5-Piperazinedione,1-(2-hydroxyethyl)-3,3-dimethyl-(9CI)(143411-86-3)
    12. EPA Substance Registry System: 2,5-Piperazinedione,1-(2-hydroxyethyl)-3,3-dimethyl-(9CI)(143411-86-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 143411-86-3(Hazardous Substances Data)

143411-86-3 Usage

Structure

Cyclic amide containing a piperazine ring and a 2-hydroxyethyl group

Usage

Synthesis of various pharmaceuticals and organic compounds, potential applications in medicinal chemistry

Biological activities

Potential antitumor and antibacterial properties

Additional studies needed

To fully understand the potential uses and properties of the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 143411-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,4,1 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 143411-86:
(8*1)+(7*4)+(6*3)+(5*4)+(4*1)+(3*1)+(2*8)+(1*6)=103
103 % 10 = 3
So 143411-86-3 is a valid CAS Registry Number.

143411-86-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-hydroxyethyl)-3,3-dimethylpiperazine-2,5-dione

1.2 Other means of identification

Product number -
Other names 1-(2-hydroxyethyl)--dimethylpiperazine-2,5-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:143411-86-3 SDS

143411-86-3Downstream Products

143411-86-3Relevant articles and documents

ANTIMICROBIAL POLYETHER AND POLYOL COMPOUNDS

-

Page/Page column 131, (2012/05/05)

The present application describes compounds of Formula I and Formula IA and as disclosed herein, that are useful as anti-microbial agents, including as antibacterial, disinfectant, antifungal, germicidal or antiviral agents.

Novel N-chloroheterocyclic antimicrobials

Francavilla, Charles,Turtle, Eric D.,Kim, Bum,O'Mahony, Donogh J.R.,Shiau, Timothy P.,Low, Eddy,Alvarez, Nichole J.,Celeri, Chris E.,D'Lima, Louisa,Friedman, Lisa C.,Ruado, Francis S.,Xu, Ping,Zuck, Meghan E.,Anderson, Mark B.,Najafi, Ramin,Jain, Rakesh K.

scheme or table, p. 3029 - 3033 (2011/06/24)

Antimicrobial compounds with broad-spectrum activity and minimal potential for antibiotic resistance are urgently needed. Toward this end, we prepared and investigated a novel series of N-chloroheterocycles. Of the compounds examined, the N-chloroamine series were found superior over N-chloroamide series in regards to exhibiting high antimicrobial activity, low cytotoxicity, and long-term aqueous stability.

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