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2,3,5,6-tetrachloro-4-[(2-cyanoethyl)sulfonyl]benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56916-60-0

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56916-60-0 Usage

Explanation

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

Explanation

The compound has four chlorine atoms, a benzene ring with a nitrile group (CN), a sulfonyl group (SO2), and a cyanoethyl side chain (C2H4N).

Explanation

It is mainly used to control the growth of unwanted plants.

Explanation

The compound is applied before the emergence of weeds to prevent their growth in ornamental plants and turf grasses.

Explanation

The compound interferes with the normal functioning of the weeds' biochemical processes, preventing their growth and development.

Explanation

The compound poses a significant risk to aquatic life due to its high toxicity and tendency to remain in the environment for a long time.

Explanation

Due to its high toxicity and environmental persistence, the compound is considered hazardous and requires special handling, use, and disposal procedures.

Explanation

To minimize the risk of harm to human health and the environment, it is essential to follow safety guidelines and protocols when handling, using, and disposing of the compound.

Structure

Tetrachloro-substituted benzonitrile derivative with a sulfonyl group and a cyanoethyl side chain

Primary use

Herbicide

Application

Pre-emergent weed control agent for ornamental plants and turf grasses

Mode of action

Inhibits the growth of weeds at their earliest stages by disrupting essential biochemical processes

Environmental impact

High toxicity to aquatic organisms and potential for environmental persistence

Hazard classification

Classified as a hazardous substance

Precautions

Strict precautions must be taken during handling, use, and disposal

Check Digit Verification of cas no

The CAS Registry Mumber 56916-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,1 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56916-60:
(7*5)+(6*6)+(5*9)+(4*1)+(3*6)+(2*6)+(1*0)=150
150 % 10 = 0
So 56916-60-0 is a valid CAS Registry Number.

56916-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,6-tetrachloro-4-(2-cyanoethylsulfonyl)benzonitrile

1.2 Other means of identification

Product number -
Other names BENZONITRILE,4-CYANOETHYLSULFONYL-2,3,5,6-TETRACHLORO

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:56916-60-0 SDS

56916-60-0Downstream Products

56916-60-0Relevant academic research and scientific papers

Synthesis and antiinflammatory evaluation of substituted isophthalonitriles, trimesonitriles, benzonitriles, and terephthalonitriles

Heilman,Battershell,Pyne,Goble,Magee

, p. 906 - 913 (2007/10/06)

In an effort to develop nonacidic, nonsteroidal, antiinflammatory agents without gastrointestinal complications, a series of cyanobenzenes was synthesized for antiinflammatory evaluation. Twenty-seven substituted isophthalonitriles, 19 trimesonitriles, 30 benzonitriles, and 16 terephthalonitriles were tested in the rat utilizing the carrageenan-induced pedal edema assay. Based on the performance of phenylbutazone in this assay (43.8% reduction at 100 mg/kg), six compounds, dosed at 50 mg/kg, produced reductions in inflammation comparable to this standard. However, the LD50 value of each compound dosed at this level was in the range of 40-56 mg/kg in the mouse; therefore, further study was not warranted. Fifteen compounds possessed activity in excess of 20% reduction at 200 mg/kg and also possessed LD50 values greater than 300 mg/kg. Of these cyanobenzenes, trimesonitrile, 4-chlorobenzonitrile, 2-chloroterephthalonitrile, and 2-fluoroterephthalonitrile with reductions in edema of 32, 30, 46, and 49%, respectively, represent the best candidates for subsequent study.

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