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(5Z)-1,1-dimethyl-3-oxo-4-(propan-2-yl)-5-(propan-2-ylimino)-1,2,4-triazolidin-1-ium is a complex organic compound characterized by a 1,2,4-triazolidin-1-ium core. It is a derivative of triazolidine, featuring a unique heterocyclic ring structure. This specific compound is distinguished by the presence of a propan-2-ylimino group and a propan-2-yl group at the 5-position, along with a ketone group at the 3-position. With a molecular formula of C9H18N3O and a Z-configuration, it holds potential for applications in organic synthesis, medicinal chemistry, and other areas that can benefit from its distinctive structural and chemical properties.

32515-30-3

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32515-30-3 Usage

Uses

Used in Organic Synthesis:
(5Z)-1,1-dimethyl-3-oxo-4-(propan-2-yl)-5-(propan-2-ylimino)-1,2,4-triazolidin-1-ium is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for multiple points of reactivity, making it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (5Z)-1,1-dimethyl-3-oxo-4-(propan-2-yl)-5-(propan-2-ylimino)-1,2,4-triazolidin-1-ium is utilized as a potential lead compound for the development of new drugs. Its heterocyclic core and functional groups can be optimized to target specific biological receptors or enzymes, contributing to the discovery of novel therapeutic agents.
Used in Chemical Research:
(5Z)-1,1-dimethyl-3-oxo-4-(propan-2-yl)-5-(propan-2-ylimino)-1,2,4-triazolidin-1-ium serves as a subject of study in chemical research, where its properties, reactivity, and behavior in various chemical reactions are investigated. This research can lead to a deeper understanding of triazolidine chemistry and inspire the design of new compounds with improved or novel functionalities.
Used in Specialty Chemicals Industry:
(5Z)-1,1-dimethyl-3-oxo-4-(propan-2-yl)-5-(propan-2-ylimino)-1,2,4-triazolidin-1-ium is also used in the specialty chemicals industry for the development of high-value products with specific applications. Its unique structure and properties can be tailored to meet the needs of various industries, such as materials science, where it could be used to create new polymers or other advanced materials with specialized properties.

Check Digit Verification of cas no

The CAS Registry Mumber 32515-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,5,1 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32515-30:
(7*3)+(6*2)+(5*5)+(4*1)+(3*5)+(2*3)+(1*0)=83
83 % 10 = 3
So 32515-30-3 is a valid CAS Registry Number.

32515-30-3SDS

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 1,1-dimethyl-4-propan-2-yl-5-propan-2-ylimino-1,2,4-triazol-1-ium-3-olate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:32515-30-3 SDS

32515-30-3Relevant academic research and scientific papers

The Photolysis of Carbamoyl Azides in the Presence of Carbodiimides

Lwowski, Walter,Kanemasa, Suji,Murray, Roy A.,Ramakrishnan, V. T.,Thiruvengadam, T. K.,et al.

, p. 1719 - 1723 (2007/10/02)

The photolysis of some N,N-dialkylcarbamoyl azides in the presence of carbodiimides gives two types of products: cyclic ammonio amates 1 (from N,N-dialkylamino isocyanates, formed by a photo-Curtius rearrangement of the azides) and five-membered mesoinoic 5-(dialkylamino)-1,2,4-triazoles 7, the structure of which was confirmed by independent synthesis.The formation of 7 constitutes a novel reaction path of carbamoyl azides.

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