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597559-60-9

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597559-60-9 Usage

Explanation

The molecular formula represents the numbers of atoms of each element present in a molecule of the compound.

Explanation

The physical state and color of the compound when it is in its pure form.

Explanation

The primary applications of the compound in the agricultural industry.

Explanation

The classification of the compound based on its chemical structure and mode of action.

Explanation

The specific types of weeds that the compound is effective in controlling.

Explanation

The biological process that the compound interferes with, leading to the death of the plant.

Explanation

The possible negative impacts on the environment and human health due to the use of the compound.

Explanation

The legal restrictions and guidelines in place to control the use of the compound to minimize its potential risks.

Appearance

White solid

Usage

Pesticide and herbicide

Category

Triazine herbicide

Target

Broadleaf and grassy weeds

Mode of action

Inhibits photosynthesis in plants

Environmental and health risks

Potential risks

Regulation

Use and application are regulated in many countries

Check Digit Verification of cas no

The CAS Registry Mumber 597559-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,7,5,5 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 597559-60:
(8*5)+(7*9)+(6*7)+(5*5)+(4*5)+(3*9)+(2*6)+(1*0)=229
229 % 10 = 9
So 597559-60-9 is a valid CAS Registry Number.

597559-60-9Relevant articles and documents

Novel syntheses of the amino-1,2,4-triazine GW356194: Identification of a synthesis amenable to scale up

Adam, Fiona M.,Burton, Andrew J.,Cardwell, Kevin S.,Cox, Richard A.,Henson, Richard A.,Mills, Keith,Prodger, Jeremy C.,Schilling, Mark B.,Tape, Daniel T.

, p. 5657 - 5659 (2007/10/03)

New syntheses of the amino-1,2,4-triazine, GW356194 have been developed to improve on existing methodology. The use of different amidrazones in cyclisations with α-keto and α-amido carbonyl compounds as the key step for the synthesis of the 1,2,4-triazine core was evaluated and the results are presented here.

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