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2,6-dichloro-N-[(4-chlorophenyl)carbamoyl]benzamide is a chemical compound with the molecular formula C13H8Cl3N3O2. It is an amide derivative of benzamide, characterized by the presence of two chlorine atoms, a chlorophenyl group, and a carbamoyl group attached to a benzene ring structure. 2,6-dichloro-N-[(4-chlorophenyl)carbamoyl]benzamide is known for its potent herbicidal and pesticidal properties, making it a valuable agent in agricultural and environmental research applications.

35409-97-3

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35409-97-3 Usage

Uses

Used in Agricultural Industry:
2,6-dichloro-N-[(4-chlorophenyl)carbamoyl]benzamide is used as a herbicide for its effective weed-killing properties, targeting the inhibition of unwanted plant growth by disrupting their cellular processes. This helps in maintaining the health and productivity of crops by reducing competition for resources and preventing the spread of plant diseases.
Used in Pest Control:
In the pest control industry, 2,6-dichloro-N-[(4-chlorophenyl)carbamoyl]benzamide serves as a pesticide, combating pests that can damage crops and reduce agricultural yields. Its ability to disrupt the cellular processes of pests makes it a potent tool in protecting crops from infestations.
Used in Scientific Research:
2,6-dichloro-N-[(4-chlorophenyl)carbamoyl]benzamide is also utilized in scientific research as a tool for investigating the effects of herbicides and pesticides on crops and the environment. This helps in understanding the mechanisms of action, potential side effects, and the development of more effective and environmentally friendly alternatives.

Check Digit Verification of cas no

The CAS Registry Mumber 35409-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,0 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35409-97:
(7*3)+(6*5)+(5*4)+(4*0)+(3*9)+(2*9)+(1*7)=123
123 % 10 = 3
So 35409-97-3 is a valid CAS Registry Number.

35409-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dichlorbenzuron

1.2 Other means of identification

Product number -
Other names PH 60-38

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:35409-97-3 SDS

35409-97-3Relevant academic research and scientific papers

Enhancement of seed yield of soybeans by a substituted benzoyl urea

-

, (2008/06/13)

A method is disclosed for increasing yield in soybeams by applying, in the absence of insect pressure on the crop, an amount effective for increasing seed pod formation of an active amount of a substituted benzoyl urea represented by structural formula (I).

Enhancement of insecticides activity on Bt cotton

-

, (2008/06/13)

A method for controlling insects of Lepidoptera on a genetically altered cotton plant having incorporated therein a gene derived from Bacillus thuringiensis (Bt) which codes for and expresses a protein having pesticide activity comprising the steps of applying to the foliage of said genetically altered cotton plant a pesticidally active amount of certain substituted benzoyl urea compounds.

KINETICS OF METHANOLYSIS OF 1-(2-HALOGENO AND 2,6-DIHALOGENOBENZOYL)-3-(4-CHLOROPHENYL)UREAS

Kavalek, Jaromir,Kacetl, Lubomir,Kavalkova, Marcela

, p. 1363 - 1369 (2007/10/02)

The methanolysis kinetics has been measured of 1-(2,6-difluorobenzoyl)-3-(4-chlorophenyl)urea (a larvicidal insecticide Dimilin) and of four other mono- and dihalogenobenzoyl derivatives.Polar and steric effects of halogen on the rate and dissociation constants is discussed.

Substituted benzoyl ureas

-

, (2008/06/13)

New organic compounds derived from urea or thiourea, insecticidal preparations on the basis of the new substances and methods of producing the substances.

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