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2,4-Dichloro-5-(2-propyloxy)acetanilide is a chemical compound with the molecular formula C13H16Cl2N2O3. It is a derivative of acetanilide, characterized by the presence of two chlorine atoms at the 2nd and 4th positions, and a 2-propyloxy group attached to the 5th position. 2,4-DICHLORO-5-(2-PROPYLOXY)ACETANILIDE is known for its application in agriculture, where it plays a crucial role in controlling the growth of unwanted plants.

65948-71-2

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65948-71-2 Usage

Uses

Used in Agricultural Applications:
2,4-Dichloro-5-(2-propyloxy)acetanilide is used as an herbicide for the selective control of broadleaf weeds. It functions by inhibiting the growth hormone auxin, which disrupts the growth of the target plants and ultimately leads to their death. This selective action makes it a valuable tool in maintaining the health and productivity of crops by eliminating competing weeds.
Used in Plant Growth Regulation:
In addition to its herbicidal properties, 2,4-Dichloro-5-(2-propyloxy)acetanilide is also employed as a plant growth regulator. It can be used to manage the growth of certain plants, ensuring that they develop in a controlled and predictable manner. This can be particularly useful in horticulture and landscaping, where precise control over plant growth is often desired.
Safety Considerations:
It is important to handle 2,4-Dichloro-5-(2-propyloxy)acetanilide with caution, as it can pose health risks if it comes into contact with the skin or if it is ingested. To minimize potential hazards, proper safety measures should be taken when using and storing this chemical compound. This includes wearing protective clothing, such as gloves and goggles, and ensuring that the substance is stored in a secure and well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 65948-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,4 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65948-71:
(7*6)+(6*5)+(5*9)+(4*4)+(3*8)+(2*7)+(1*1)=172
172 % 10 = 2
So 65948-71-2 is a valid CAS Registry Number.

65948-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,4-dichloro-5-propan-2-yloxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names OR2568

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:65948-71-2 SDS

65948-71-2Relevant academic research and scientific papers

A method for synthesizing intermediate oxadiazon

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Paragraph 0070; 0087; 0099-0104; 0110; 0120-0125; 0132; 0142, (2019/07/04)

The invention discloses a method for synthesizing intermediate oxadiazon, comprises the following steps: takes amino phenol as an initial raw material; to m-aminophenol acylation reaction is carried out, thereby obtaining a reaction solution A; the reaction solution A to proceed chlorination reaction, to obtain 2, 4 - dichloro - 5 hydroxy acetanilide; to the 2, 4 - dichloro - 5 hydroxy acetanilide etherification reaction, to obtain 2, 4 - dichloro - 5 isopropoxy acetanilide; to the 2, 4 - dichloro - 5 isopropoxy acetyl aniline to deprotected, get 2, 4 - dichloro - 5 isopropoxyaniline. The invention of 2, 4 - dichloro - 5 - isopropoxy aniline synthesis method to avoid the pollution of the environment, but there are few process steps, high yield.

Herbicidal 2-aryl-1,2,4-triazine-3,5(2H,4H)-diones and sulfur analogs thereof

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, (2008/06/13)

Herbicidal utility for 2-aryl-1,2,4-triazine-3,5(2H,4H)-diones and sulfur analogs is disclosed and exemplified. Many of the disclosed compounds are novel. Methods for preparing the herbicidal compounds and intermediates therefor are also disclosed.

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