38652-14-1

Usage

Uses

Used in Pharmaceutical Research:
1-(4-Hydroxyphenyl)-3-Methylurea is used as a potential antineoplastic agent for its capacity to inhibit the growth of cancer cells. It is valued for its mechanism of action that disrupts DNA synthesis and cell division, offering a promising avenue for the development of new cancer treatments.
Used in Cancer Treatment Development:
In the field of oncology, 1-(4-Hydroxyphenyl)-3-Methylurea is utilized as a research compound to explore its potential in treating various types of cancer. Its ability to interfere with essential cellular processes makes it a candidate for further investigation into its therapeutic efficacy and possible integration into cancer treatment protocols.
Used in Research for Other Medical Conditions:
Beyond its antineoplastic properties, 1-(4-Hydroxyphenyl)-3-Methylurea is also studied for its potential applications in managing other medical conditions such as diabetes and cardiovascular diseases. This underscores the compound's versatility and the breadth of its potential impact on healthcare and biomedical research.

InChI:InChI=1/C8H10N2O2/c1-9-8(12)10-6-2-4-7(11)5-3-6/h2-5,11H,1H3,(H2,9,10,12)

Upstream product

• 34123-59-6 N-(4-isopropylphenyl)-N',N'-dimethylurea 
• 51-78-5 p-aminophenol hydrochloride 
• 624-83-9 methyl isocyanate 
• 123-30-8 4-amino-phenol 
• 150-68-5 monuron 

Downstream Products

• 38649-71-7 1-[4-(3-tert-Butylamino-2-hydroxy-propoxy)-phenyl]-3-methyl-urea 
• 76210-75-8 4-(2-{2-Hydroxy-3-[4-(3-methyl-ureido)-phenoxy]-propylamino}-ethoxy)-benzamide 
• 76210-79-2 1-(4-{3-[2-(3,4-Dimethoxy-phenyl)-ethylamino]-2-hydroxy-propoxy}-phenyl)-3-methyl-urea 

Relevant academic research and scientific papers

The effect of natural iron oxide and oxalic acid on the photocatalytic degradation of isoproturon: A kinetics and analytical study

The photocatalytic degradation of isoproturon, a persistent toxic herbicide, was investigated in the presence of natural iron oxide and oxalic acid and under UV irradiation. The influence of the relevant parameters such as the pH and the iron oxide and oxalic acid concentrations has been studied. The presence of natural iron oxide and oxalic acid in the system effectively allow the degradation of isoproturon, whereas the presence of t-butyl alcohol adversely affects the phototransformation of the target pollutant, thus indicating that an OH radical initiated the degradation mechanism. The degradation mechanism of isoproturon was investigated by means of GC-MS analysis. Oxidation of both the terminal N-(CH3)2 and isopropyl groups is the initial process leading to N-monodemethylated (NHCH3), N-formyl (N(CH3)CHO), and CHCH3OH as the main intermediates. The substitution of the isopropyl group by an OH group is also observed as a side process.

Kinetic and analytical study of the photo-induced degradation of monuron by nitrates and nitrites under irradiation or in the dark

The photo-induced transformation of monuron (3-(4-chlorophenyl)-1,1 dimethylurea) was investigated in an aqueous solution containing nitrates and nitrites at 310 nm and 365 nm, respectively. In both NO3- and NO2-/sup

Anti-coccidal agents 1-[4-(benzothia- or -oxazol-2-ylthio- or -2-yloxy)phenyl]-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione derivatives, compositions, and method of use thereof

1-[4-(Benzothia- or -oxazol-2-ylthio- or -2-yloxy)phenyl]-1,3,5-triazine-2,4,6(1H,3H,5H)-triones of the formula STR1 in which R is lower alkyl, R1 and R2 each independently is hydrogen, halogen, alkyl or alkoxy, R3 and Rs

1-Methoxy-1-methyl-3-{p-[(1,1-dimethyl-2-propynyloxy)-methoxy]phenyl}urea

This invention relates to novel (alkenyloxy), (alkynyloxy) and (cyanoalkoxy) alkoxyphenyl ureas and their use as herbicidal agents.