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1003-34-5

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1003-34-5 Usage

Description

5-chloro-2,4-dihydro-3H-1,2,4-triazol-3-one (SALTDATA: FREE) is a chemical compound characterized by its molecular formula C2H2ClN3O. It is a white crystalline solid with a slightly bitter taste, exhibiting solubility in water and alcohol. This versatile compound is recognized for its diverse applications across various industries.

Uses

Used in Pharmaceutical Industry:
5-chloro-2,4-dihydro-3H-1,2,4-triazol-3-one (SALTDATA: FREE) is used as an intermediate in the manufacturing of pharmaceuticals for its potential to contribute to the development of new drugs.
Used in Pesticide Industry:
In the pesticide industry, 5-chloro-2,4-dihydro-3H-1,2,4-triazol-3-one (SALTDATA: FREE) is utilized as an intermediate, playing a role in the synthesis of active ingredients for pest control.
Used in Dye Industry:
5-chloro-2,4-dihydro-3H-1,2,4-triazol-3-one (SALTDATA: FREE) is employed as an intermediate in the production of dyes, contributing to the creation of colorants for various applications.
Used as a Herbicide:
5-chloro-2,4-dihydro-3H-1,2,4-triazol-3-one (SALTDATA: FREE) is used as a herbicide to control, inhibit, or kill unwanted plants in agricultural settings.
Used as a Plant Growth Regulator:
5-chloro-2,4-dihydro-3H-1,2,4-triazol-3-one(SALTDATA: FREE) also serves as a plant growth regulator, influencing the growth and development of plants in a controlled manner.
Used in Biological Research:
5-chloro-2,4-dihydro-3H-1,2,4-triazol-3-one (SALTDATA: FREE) has shown promise in biological research as a potential antifungal and antimicrobial agent, indicating its use in the study and development of treatments for fungal and microbial infections.
It is important to follow proper handling and usage precautions when working with 5-chloro-2,4-dihydro-3H-1,2,4-triazol-3-one (SALTDATA: FREE) to ensure safety and prevent any adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 1003-34-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1003-34:
(6*1)+(5*0)+(4*0)+(3*3)+(2*3)+(1*4)=25
25 % 10 = 5
So 1003-34-5 is a valid CAS Registry Number.

1003-34-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-1,2-dihydro-1,2,4-triazol-3-one

1.2 Other means of identification

Product number -
Other names 5-chloro-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:1003-34-5 SDS

1003-34-5Downstream Products

1003-34-5Relevant articles and documents

Synthesis of [3-14C]- and [5-14C]-labelled 5-nitro-1,2,4-triazol-3-one (NTO) and study of its chemical decomposition

Le Campion,De Suzzoni-Dezard,Robic,Vandais,Varenne,Noel,Ouazzani

, p. 1203 - 1213 (2007/10/03)

The chemical decomposition of NTO 1 and its corresponding amine ATO 2 was investigated. To make easier the identification of the decomposition products, we synthesized 14C-labelled NTO and ATO. Our results confirmed the high stability of the NTO triazolone ring. Its scission can be achieved partially by sulfuric acid under intensive heat and pressure. The triazolone ring of ATO was cleaved in alkaline solution. Carbon dioxide is evolved leaving a polar compound assumed to be aminoguanidine. The deamination of ATO was achieved by nitrosation. In dilute HCl (0.15 N), 2 equivalents of NO2- led to the triazolone 4, through a radical de-diazotation of the diazo intermediate. With 3 to 10 equivalents of NO2-, the nitrosation leads exclusively to the azide 6.

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