10242-18-9 Usage
Uses
Used in Chemical Synthesis:
2,4-dinitro-1-(prop-2-en-1-yloxy)benzene is used as an intermediate for the synthesis of various organic compounds, contributing to the production of a wide range of chemical products.
Used in Chemical Reactions:
2,4-dinitro-1-(prop-2-en-1-yloxy)benzene also serves as a reagent in chemical reactions, playing a crucial role in the formation of new compounds and facilitating various chemical processes.
Used in Pesticide and Herbicide Applications:
2,4-dinitro-1-(prop-2-en-1-yloxy)benzene is used as a pesticide and herbicide, primarily for controlling broadleaf weeds in various crops. Its effectiveness in managing unwanted plant growth makes it a valuable tool in agricultural practices.
Used in Agricultural Industry:
In the agricultural industry, 2,4-dinitro-1-(prop-2-en-1-yloxy)benzene is used as a herbicidal agent for controlling broadleaf weeds, ensuring the healthy growth of crops and increasing yield.
Safety Precautions:
It is important to handle 2,4-dinitro-1-(prop-2-en-1-yloxy)benzene with care, as it is toxic to humans and can cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken to minimize exposure and potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 10242-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,4 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10242-18:
(7*1)+(6*0)+(5*2)+(4*4)+(3*2)+(2*1)+(1*8)=49
49 % 10 = 9
So 10242-18-9 is a valid CAS Registry Number.
10242-18-9Relevant academic research and scientific papers
THERAPEUTIC DNP DERIVATIVES AND METHODS USING SAME
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Page/Page column 56; 57; 58, (2015/03/16)
The present invention includes DNP derivatives that are useful for preventing or treating a metabolic disease or disorder in a subject in need thereof. In certain embodiments, the subject is further administered at least one additional therapeutic agent.
Hydrolysis of ethers of 2,4-dinitrophenol. No evidence for a single electron transfer mechanism
De Vargas,Setti,Aimar,De Rossi
, p. 7364 - 7367 (2007/10/02)
The reactions of 3-butenyl 2,4-dinitrophenyl ether (1), allyl 2,4- dinitrophenyl ether (5), and n-butyl 2,4-dinitrophenyl ether (6) with KOH in two DMSO-water mixtures (50% v/v and 70% v/v) were studied. In all cases, no evidence was found for a single electron transfer mechanism; 2,4- dinitrophenol was the only product formed. The reaction follows the classical S(N)Ar mechanism. The order of reactivity is 5 > 1 > 6 in both solvents, although the reactivities differ only by factors of 1.4 and 2 in 50 and 70% DMSO, respectively.
