15302-91-7 Usage
Uses
Used in Agriculture:
Mepiquat is used as a plant growth inhibitor to control the growth of plants, particularly in the agricultural industry. It helps in reducing the excessive growth of plants, which can be beneficial for crop management and yield optimization.
Used in Horticulture:
In the horticulture industry, Mepiquat is used as a growth regulator to maintain the desired size and shape of plants, especially in ornamental and landscape settings. It can help in preventing the overgrowth of plants and maintaining their aesthetic appeal.
Used in Research:
Mepiquat is also used as a research tool in the field of plant biology and agriculture. It helps scientists study the effects of growth regulation on plant development and can be used to investigate the mechanisms behind plant growth inhibition.
Check Digit Verification of cas no
The CAS Registry Mumber 15302-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,0 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15302-91:
(7*1)+(6*5)+(5*3)+(4*0)+(3*2)+(2*9)+(1*1)=77
77 % 10 = 7
So 15302-91-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N.ClH/c1-8(2)6-4-3-5-7-8;/h3-7H2,1-2H3;1H/q+1;/p-1
15302-91-7Relevant academic research and scientific papers
Reactions of Nitroanisoles. Part 2. Reactions of 2,4- and 2,6-Dinitroanisole with Piperidines in Benzene
Nudelman, N. Sbarbati,Palleros, Daniel
, p. 995 - 999 (2007/10/02)
The reactions of 2,4- (I) and 2,6-dinitroanisole (VIII) with piperidine (II) and N-methylpiperidine (NMP) in benzene have been studied.It was found that (I) and (VIII) react with (II) to give not only the expected aromatic nucleophilic substitution (a.n.s.) products, but also the corresponding dinitrophenols, generated by an SN2 reaction.The rate for each reaction and the overall rates were measured and it was observed that compound (I) has similar rate coefficients for the a.n.s. as well as for the SN2 reaction.Mild acceleration by base was found for the a.n.s.reaction.When (VIII) reacts with (II) the rate of reaction to form 2,6-dinitrophenol is greater than the rate for the a.n.s.In the reaction with NMP only an SN2 reaction was observed.Furthermore, the rates of reaction of (VIII) with (II) and with NMP are ca. 1000 and 300 times, respectively, the rate of reaction of (I) with these amines.A field effect is proposed for the increase in rate.