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1H-[1,2,4]Triazole-3-carboxylic acid hydrazide is a chemical compound characterized by its molecular formula C3H4N6O2. It is a hydrazide derivative of 1H-[1,2,4]Triazole-3-carboxylic acid, known for its triazole ring that endows the molecule with distinctive properties and reactivity. 1H-[1,2,4]Triazole-3-carboxylic acid hydrazide is frequently utilized as a fundamental building block in the synthesis of pharmaceuticals and agrochemicals, owing to its potential for further functionalization and the creation of a variety of chemical structures.

21732-98-9

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21732-98-9 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
1H-[1,2,4]Triazole-3-carboxylic acid hydrazide is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to contribute to the development of new molecules with potential therapeutic or pesticidal properties.
Used in Research and Development:
In the realm of research and development, 1H-[1,2,4]Triazole-3-carboxylic acid hydrazide is employed as a precursor in the preparation of chemical libraries for drug discovery. Its versatility in forming heterocyclic compounds makes it a valuable asset in exploring novel chemical entities with potential applications in medicine and agriculture.
Used in Heterocyclic Chemistry:
1H-[1,2,4]Triazole-3-carboxylic acid hydrazide is utilized as a starting material for the synthesis of other heterocyclic compounds, leveraging its hydrazide functionality to enable the creation of diverse and complex chemical structures that can be further explored for their properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 21732-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,3 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21732-98:
(7*2)+(6*1)+(5*7)+(4*3)+(3*2)+(2*9)+(1*8)=99
99 % 10 = 9
So 21732-98-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H5N5O/c4-7-3(9)2-5-1-6-8-2/h1H,4H2,(H,7,9)(H,5,6,8)

21732-98-9SDS

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 1H-1,2,4-triazole-5-carbohydrazide

1.2 Other means of identification

Product number -
Other names 1H-1,2,4-triazole-3-carbohydrazide

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:21732-98-9 SDS

21732-98-9Relevant academic research and scientific papers

CHEMICAL FOAMING AGENTS CONTAINING TOSYL GROUPS

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Paragraph 0073, (2021/08/27)

Chemical foaming agents having p-toluenesulfonyl groups. Processes for preparing foamed polyolefin compositions using chemical foaming agents having p-toluenesulfonyl groups. Articles of manufacture containing formed polyolefins prepared using chemical foaming agents having p-toluenesulfonyl groups.

Dinuclear, tetranuclear and chain (MnII, CoII) complexes of multifunctional hydrazone ligands- Structural and magnetic studies

Bettle, Peter J.,Dawe, Louise N.,Anwar, Muhammad U.,Thompson, Laurence K.

experimental part, p. 5036 - 5042 (2012/01/14)

The coordination chemistry of a group of hydrazone-based ligands, modified with carboxylate and heterocyclic terminal donor groups, with MnII and CoII has been investigated. The multifunctional nature of the ligands allows coordinative flexibility based on the hydrazone core, which is well established to lead to spin-coupled polymetallic assemblies through μ-Ohydrazone bridging. Examples of dinuclear, tetranuclear and chain complexes are reported with hydrazone, carboxylate and triazole bridging. Spin exchange through the μ-O and μ-N,N bridging connections leads to antiferromagnetic exchange in most cases, except for the central subunit in the MnII4 chain complex, where small ( 90°) bridge angles result in contributing ferromagnetic interactions. Multifunctional polytopic hydrazone ligands form polymetallic complexes with μ-O (hydrazone, carboxylate) and μ-N,N (triazole) bridging, leading to spin-spin interactions between the metal centres with examples of antiferromagnetic and ferromagnetic exchange.

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