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Bentazone Methyl Derivative is a chemical compound derived from Bentazon, a widely used herbicide for controlling broadleaf and grassy weeds in various crops. This derivative exhibits similar properties to its parent compound, with potential applications in agriculture for weed management. It is characterized by its chemical structure, which includes a methyl group attached to the Bentazon molecule, altering its physical and chemical properties. The derivative may offer advantages such as improved solubility, stability, or selectivity in certain agricultural settings. However, it is important to note that the specific benefits and drawbacks of Bentazon Methyl Derivative would be determined through detailed chemical analysis and field testing, as the impact of the methyl group on the herbicidal activity and environmental behavior can vary.

2225-40-3

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2225-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2225-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2225-40:
(6*2)+(5*2)+(4*2)+(3*5)+(2*4)+(1*0)=53
53 % 10 = 3
So 2225-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O3S/c1-10-8(11)6-4-2-3-5-7(6)9-14(10,12)13/h2-5,9H,1H3

2225-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2,2-dioxo-1H-2λ<sup>6</sup>,1,3-benzothiadiazin-4-one

1.2 Other means of identification

Product number -
Other names N-methyl-bentazon

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:2225-40-3 SDS

2225-40-3Downstream Products

2225-40-3Relevant academic research and scientific papers

KINETICS AND MECHANISM OF CYCLIZATION OF N-(2-METHOXYCARBONYLPHENYL)-N'-METHYLSULFONAMIDE TO 3-METHYL-(1H)-2,1,3-BENZOTHIADIAZIN-4(3H)-ONE 2,2-DIOXIDE

Kavalek,Jaromir,Machacek, Vladimir,Sedlak, Milos,Sterba, Vojeslav

, p. 1701 - 1710 (2007/10/02)

The cyclization kinetics of N-(2-methoxycarbonylphenyl)-N'-methylsulfonamide (IIb) into 3-methyl-(1H)-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide (Ib) has been studied in ethanolamine, morpholine, and butylamine buffers and in potassium hydroxide solutions.The cyclization is subject to general base and general acid catalysis.The value of the Broensted coefficient β is about 0.1, which indicates that splitting off of the proton from negatively charged tetrahedral intermediate represents the rate-limiting and thermodynamically favourable step.In the solutions of potassium hydroxide the cyclization of dianion of the starting ester IIb probably becomes the rate-limiting step.

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