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56957-81-4

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56957-81-4 Usage

Chemical Structure

C16H16Cl4NO2S

Usage

Herbicide for controlling grasses and broadleaf weeds in agricultural and non-agricultural settings

Mode of Action

Inhibits the photosynthesis process in plants, leading to their death

Environmental Impact

Persistent in the environment, potential to bioaccumulate, poses a risk to aquatic and terrestrial organisms

Health Risks

Potential to cause harm to human health

Regulation

Classified as a restricted use pesticide in some regions

Handling and Disposal

Proper handling and disposal practices are crucial to minimize its impact on the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 56957-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,5 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56957-81:
(7*5)+(6*6)+(5*9)+(4*5)+(3*7)+(2*8)+(1*1)=174
174 % 10 = 4
So 56957-81-4 is a valid CAS Registry Number.

56957-81-4SDS

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 2,3,5,6-tetrachloro-4-decylsulfonylbenzonitrile

1.2 Other means of identification

Product number -
Other names Benzonitrile,4-(decylsulfonyl)-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:56957-81-4 SDS

56957-81-4Downstream Products

56957-81-4Relevant articles and documents

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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