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N-carbamoyl-2-(2,4-dichlorophenoxy)acetamide is a chemical compound with the molecular formula C9H8Cl2N2O3. It is an amide derivative, characterized by the presence of a carbamoyl group (-CONH2) and a 2,4-dichlorophenoxy group attached to the acetamide moiety. N-carbamoyl-2-(2,4-dichlorophenoxy)acetamide is known for its herbicidal properties, particularly as a selective herbicide used in agriculture to control broadleaf and grassy weeds. It functions by inhibiting the enzyme acetohydroxyacid synthase, which is crucial for plant growth, thus preventing the synthesis of essential amino acids and leading to the death of the plant. The chemical's specific structure and activity make it a valuable tool in modern agriculture for managing weed populations and protecting crop yields.

5205-43-6

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5205-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5205-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,0 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5205-43:
(6*5)+(5*2)+(4*0)+(3*5)+(2*4)+(1*3)=66
66 % 10 = 6
So 5205-43-6 is a valid CAS Registry Number.

5205-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-carbamoyl-2-(2,4-dichlorophenoxy)acetamide

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5205-43-6 SDS

5205-43-6Relevant academic research and scientific papers

Synthesis of nitrogen-containing phenoxyacetic acid derivatives

Yamansarova,Kukovinets,Zainullin,Galin,Abdullin

, p. 546 - 550 (2007/10/03)

Nitrogen-containing phenoxyacetic acid derivatives were synthesized by reactions of substituted phenoxyacetic acids with amines, urea, and ethyl carbamate.

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