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Benzene, 1,3-dichloro-2-(2,4-dichlorophenoxy)-, commonly known as dicamba, is a chemical compound that functions as an herbicide. It is designed to control broadleaf weeds in various agricultural settings by disrupting plant growth and causing uncontrolled cell growth, ultimately leading to plant death.

147102-65-6

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147102-65-6 Usage

Uses

Used in Agricultural Industry:
Dicamba is used as a herbicidal agent for controlling broadleaf weeds in crops such as corn, soybeans, and wheat. Its application helps to protect and promote the growth of desired crops by eliminating competing weeds.
Used in Lawn Care Products:
In addition to agricultural applications, dicamba is also utilized in lawn care products to manage broadleaf weeds, ensuring a healthy and visually appealing lawn.
However, it is important to note that dicamba has been a subject of controversy due to its potential to drift off-target, causing damage to neighboring crops. As a result, ongoing research and regulations are being implemented to minimize the associated risks and ensure the safe and effective use of dicamba in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 147102-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,0 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 147102-65:
(8*1)+(7*4)+(6*7)+(5*1)+(4*0)+(3*2)+(2*6)+(1*5)=106
106 % 10 = 6
So 147102-65-6 is a valid CAS Registry Number.

147102-65-6Downstream Products

147102-65-6Relevant academic research and scientific papers

Synthesis, Structure Verification, and Chromatographic Relative Retention Times for Polychlorinated Diphenyl Ethers

Nevalainen, Tapio,Koistinen, Jaana,Nurmela, Pirjo

, p. 1341 - 1347 (2007/10/03)

Fifty-four polychlorinated diphenyl ether (PCDEs) congeners were synthesized, and their structures were confirmed by mass spectrometry and proton magnetic resonance spectroscopy. The gas chromatographic relative retention times (RRT) for the PCDEs were determined relative to a reference standard, -tetrachlorobiphenyl (PCB 77) on the fused silica capillary columns of SE-54 and OV-1701. The retention times for PCDEs increased with the increasing number of vicinal chlorines within a series of isomers. The chlorine substitution patterns of PCDEs were used to develop a method for predicting RRTs for congeners that were not synthesized.

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