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1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium, a cationic triazolidine derivative with the molecular formula C8H15N3O2, is a stable chemical compound under standard conditions. It is characterized by a positively charged nitrogen atom and is widely recognized for its antimicrobial properties. 1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium has found applications in various fields, including organic synthesis, pharmaceuticals, and biotechnology, making it a significant player in the realm of chemistry.

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  • 54133-08-3 Structure
  • Basic information

    1. Product Name: 1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium
    2. Synonyms:
    3. CAS NO:54133-08-3
    4. Molecular Formula: C5H9N3O2
    5. Molecular Weight: 144.1513
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54133-08-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium(54133-08-3)
    11. EPA Substance Registry System: 1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium(54133-08-3)
  • 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: 54133-08-3(Hazardous Substances Data)

54133-08-3 Usage

Uses

Used in Organic Synthesis:
1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions. Its cationic nature and unique molecular structure make it a valuable component in the creation of complex organic molecules.
Used in Pharmaceutical Applications:
1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium is used as an active ingredient in pharmaceuticals for its antimicrobial properties. It has the potential to be developed into new drugs targeting a range of bacterial and fungal infections, contributing to the ongoing fight against antibiotic resistance.
Used in Biotechnology:
In the biotechnology industry, 1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium is used as a component in the development of novel bioactive compounds. Its unique chemical properties allow it to be integrated into various biotechnological applications, such as the creation of new antimicrobial agents or the enhancement of existing ones.
Overall, 1,1,4-trimethyl-3,5-dioxo-1,2,4-triazolidin-1-ium is a versatile compound with a wide range of applications across different industries, making it an essential tool in the field of chemistry. Its stability, reactivity, and antimicrobial properties continue to drive research and development efforts, paving the way for new discoveries and innovations.

Check Digit Verification of cas no

The CAS Registry Mumber 54133-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,3 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54133-08:
(7*5)+(6*4)+(5*1)+(4*3)+(3*3)+(2*0)+(1*8)=93
93 % 10 = 3
So 54133-08-3 is a valid CAS Registry Number.

54133-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,4-trimethyl-5-oxo-1,2,4-triazol-1-ium-3-olate

1.2 Other means of identification

Product number -
Other names 1,1,4-trimethyl-1,2,4-triazolidine-3,5-dione 1,2-ylide

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:54133-08-3 SDS

54133-08-3Relevant articles and documents

Photolysis of Dimethylcarbamoyl Azide in the Presence of a Cyclic Aminimide

Gibson, Harry H.,Weissinger, Keith,Abashawl, Aida,Hall, Greg,Lawshae, Tom,et al.

, p. 3858 - 3861 (2007/10/02)

Dimethylcarbamoyl azide has been photolyzed in the presence of methyl isocyanate to produce the cyclic aminimide 1,1,4-trimethyl-1,2,4-triazolidine-3,5-dione 1,2-ylide (6) and the azo compound N-(dimethylcarbamoyl)-N,N'N'-trimethylazodicarboxamide (7).The azo compound 7 arises a photolytic reaction between dimethylcarbamoyl azide and aminimide 6.Mechanistic studies support a reaction path involving intermolecular-assisted loss of nitrogen from the azide as a result of interaction with aminimide 6.

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