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1,2,4-Triazine is an organic compound with the molecular formula C3H3N3. It is a heterocyclic compound consisting of three nitrogen atoms and three carbon atoms, forming a six-membered aromatic ring. This chemical structure endows 1,2,4-triazine with unique properties and makes it a versatile building block in various applications.

290-38-0

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290-38-0 Usage

Uses

Used in Pharmaceutical Industry:
1,2,4-Triazine is used as a valuable lead molecule for the development of new chemotherapeutic agents in human and mouse models. Its diverse pharmacological activities and easy synthetic routes make it an attractive candidate for researchers in the pharmaceutical industry.
Used in Pesticide Formulations:
1,2,4-Triazine is used as an additive in the improvement of pesticide formulations, particularly with lactamides. The incorporation of 1,2,4-triazine enhances the effectiveness and performance of these formulations, leading to better pest control and crop protection.

Check Digit Verification of cas no

The CAS Registry Mumber 290-38-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,9 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 290-38:
(5*2)+(4*9)+(3*0)+(2*3)+(1*8)=60
60 % 10 = 0
So 290-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H3N3/c1-2-5-6-3-4-1/h1-3H

290-38-0SDS

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 1,2,4-triazine

1.2 Other means of identification

Product number -
Other names [1,2,4]Triazine

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:290-38-0 SDS

290-38-0Relevant academic research and scientific papers

Preparation of tetrahydroimidazo[2,1-a]isoquinolines and their use as inhibitors of gastric acid secretion

Palmer, Andreas Marc,Grobbel, Burkhard,Brehm, Christof,Zimmermann, Peter Jan,Buhr, Wilm,Feth, Martin Philipp,Holst, Hans Christof,Simon, Wolfgang Alexander

, p. 7647 - 7660 (2008/03/28)

A series of novel tetrahydroimidazo[2,1-a]isoquinolines was prepared based on a hetero Diels-Alder reaction between an enamine and 1,2,4-triazine as key step. A structure-activity relationship was established focussing on the influence of the substitution

Trisubstituted heterocyclic compounds and their use as fungicides

-

, (2008/06/13)

Compounds of general formula (I): in which:Het represents a five or six membered saturated, partially unsaturated or aromatic ring containing between one and six heteroatoms of the group N, O, S, in which the heterocycle is substituted in an adjacent manner with -P-Q1-T-Q2, -GZ and Y, such that the substituant -GZ is adjacent to both. the other substituants being as defined in the description,process for preparing these compounds,fungicidal compositions comprising these compounds,processes for treating plants by applying these compounds or compositions.

Deamination of 2-aminothiazoles and 3-amino-1,2,4-triazines with nitric oxide in the presence of a catalytic amount of oxygen

Itoh, Takashi,Matsuya, Yuji,Nagata, Kazuhiro,Ohsawa, Akio

, p. 1547 - 1549 (2007/10/03)

2-Aminothiazoles, 2-aminobenzazoles, and 3-amino-1,2,4-triazines were deaminated using nitric oxide (NO) in the presence of a catalytic amount of oxygen to afford corresponding unsubstituted heterocycles in good yields.

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