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5-amino-1H-1,2,4-triazole-1-carboxamide is a chemical compound with the molecular formula C4H6N4O2. It is a white crystalline solid that is soluble in water and slightly soluble in ethanol. 5-amino-1H-1,2,4-triazole-1-carboxamide is primarily used as a corrosion inhibitor in various industrial applications, such as in cooling water systems and metalworking fluids, due to its ability to prevent the formation of rust and other types of corrosion. Additionally, it has been studied for its potential use as a herbicide and a plant growth regulator. The compound is also known for its ability to chelate metal ions, which can be beneficial in controlling the growth of microorganisms and algae in aquatic systems.

1489-02-7

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1489-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1489-02-7 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 1489-02:
(6*1)+(5*4)+(4*8)+(3*9)+(2*0)+(1*2)=87
87 % 10 = 7
So 1489-02-7 is a valid CAS Registry Number.

1489-02-7SDS

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 5-amino-1H-1,2,4-triazole-1-carboxamide

1.2 Other means of identification

Product number -
Other names 5-Amino-1,3-dimethyl-4-pyrazolyl o-fluorophenyl ketone

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:1489-02-7 SDS

1489-02-7Relevant 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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