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3H-1,2,4-triazol-3-one is a heterocyclic compound with the molecular formula C2H2N2O. It is a five-membered ring structure containing three nitrogen atoms and one oxygen atom, with a carbonyl group (C=O) at the 3-position. This chemical is known for its diverse applications in pharmaceuticals, agrochemicals, and materials science due to its unique reactivity and stability. It can act as a building block for the synthesis of various biologically active molecules and has been used in the development of drugs targeting a range of therapeutic areas. The compound's properties, such as its ability to form stable complexes and its potential to participate in various chemical reactions, make it a valuable component in the design and synthesis of new compounds with specific functionalities.

4045-72-1

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4045-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4045-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,4 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4045-72:
(6*4)+(5*0)+(4*4)+(3*5)+(2*7)+(1*2)=71
71 % 10 = 1
So 4045-72-1 is a valid CAS Registry Number.

4045-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4-triazol-3-one

1.2 Other means of identification

Product number -
Other names 3H-1,2,4-Triazol-3-one

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:4045-72-1 SDS

4045-72-1Downstream Products

4045-72-1Relevant academic research and scientific papers

METHODS FOR PRODUCTION OF 1,2,4-TRIAZOL-3-ONE

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Page/Page column 4-5, (2009/04/25)

Novel methods for producing 1,2,4-triazol-3-one from semicarbazide hydrochloride and formic acid are provided. In methods of this invention, water is used in removal of unreacted formic acid to increase yield and purity of produced 1,2,4-triazol-3-one.

METHODS FOR PRODUCTION OF 1,2,4-TRIAZOL-3-ONE

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Page/Page column 3-4, (2009/04/25)

Novel methods for producing 1,2,4-triazoI-3-one from semicarbazide hydrochloride and formic acid are provided. In methods of this invention, ethanol is used in removal of unreacted formic acid to increase yield and purity of produced 1,2,4-triazol-3-one.

Process for low chloride 1,2,4-triazol-5-one

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, (2008/06/13)

A process for producing 1,2,4-triazol-5-one comprises reacting a semicarbazide compound with a formic acid compound formylating agent in the presence of a catalytic amount of a sulfur-oxygen containing acid. The process is able to produce 1,2,4-triazol-5-one from semicarbazide hydrochloride having significantly lower concentrations of chloride ion, which is advantageous, for example, in the production of 3-nitro-1,2,4-triazol-5-one as an explosive used in castable explosive compositions.

Process for low chloride 1,2,4-triazol-5-one

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, (2008/06/13)

A process for producing 1,2,4-triazol-5-one reacts an aqueous hydrazine solution with urea to form a reaction mixture of semicarbazide and ammonia, the reaction mixture is concentrated and an aqueous solution of a mineral acid added to form a slurry of a salt of semicarbazide. A formic acid compound is admixed with the slurry, and the slurry heated to produce 1,2,4-triazol-5-one. The novel process results in the production of a semicarbazide salt in situ and eliminates a number of process steps required in processes of the prior art.

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