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s-Triazolo[1,5-a]-s-triazin-7(6H)-one is a heterocyclic chemical compound characterized by a distinctive three-ring structure, which includes two fused 1,2,4-triazole rings and one s-triazine ring. This nitrogen-rich molecule has garnered attention for its potential biological activities, particularly in the realm of oncology, as well as for its applications as a reducing agent and in organic synthesis.

1489-03-8

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1489-03-8 Usage

Uses

Used in Pharmaceutical Industry:
s-Triazolo[1,5-a]-s-triazin-7(6H)-one is utilized as an anticancer agent for its demonstrated effects against a variety of cancer cell lines. Its unique structure and nitrogen-based heterocycle contribute to its potential as a therapeutic agent in cancer treatment.
Used in Chemical Synthesis:
In the field of chemical synthesis, s-Triazolo[1,5-a]-s-triazin-7(6H)-one serves as a reducing agent, playing a crucial role in various chemical reactions that require the reduction of other compounds.
Used in Organic Synthesis:
s-Triazolo[1,5-a]-s-triazin-7(6H)-one is also employed in organic synthesis, where its unique structure and properties can be leveraged to create new organic compounds with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1489-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1489-03:
(6*1)+(5*4)+(4*8)+(3*9)+(2*0)+(1*3)=88
88 % 10 = 8
So 1489-03-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H3N5O/c10-4-7-1-5-3-6-2-8-9(3)4/h1-2H,(H,5,6,7,8,10)

1489-03-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [1,2,4]triazolo[1,5-a][1,3,5]triazin-7(6H)-one

1.2 Other means of identification

Product number -
Other names 6H-[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-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:1489-03-8 SDS

1489-03-8Downstream Products

1489-03-8Relevant academic research and scientific papers

Synthesis and pharmacological activity of triazolo[1,5-α]triazine derivatives inhibiting eosinophilia

Akahoshi, Fumihiko,Takeda, Shinji,Okada, Takehiro,Kajii, Masahiko,Nishimura, Hiroko,Sugiura, Masanori,Inoue, Yoshihisa,Fukaya, Chikara,Naito, Youichiro,Imagawa, Takashi,Nakamura, Norifumi

, p. 2985 - 2993 (2007/10/03)

In continuation of our previous work on eosinophilia inhibitors, we synthesized an additional series of inhibitors, which consisted of 5-amino- 1-[(methylamino)thiocarbonyl]-1H-1,2,4-triazole derivatives and a newly developed series of 1,2,4-triazolo[1,5-

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