n,n'-dimethylpropyleneurea (DMPU) is a colorless, odorless, hygroscopic liquid that is used as a solvent and a reagent in organic synthesis. It is a highly polar aprotic solvent, which means that it does not have a hydrogen atom attached to an electronegative atom. This property makes DMPU a good solvent for many organic reactions, as it does not interfere with the reaction mechanism. DMPU is also a good reagent for the synthesis of many organic compounds, such as amides, esters, and ethers. DMPU is a relatively inexpensive and readily available solvent, which makes it a popular choice for organic chemists. Its importance lies in its ability to dissolve a wide range of organic compounds, including polar and non-polar compounds. It is also a good solvent for many inorganic compounds. DMPU is studied for its ability to improve the solubility of organic compounds and its ability to promote certain organic reactions. DMPU is also used in the synthesis of pharmaceuticals, pesticides, and other chemicals. It is also used as a solvent in the production of polymers and plastics.'
N,N'-dimethylpropyleneurea: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
ID Source | ID |
---|---|
PubMed CID | 81646 |
CHEMBL ID | 12284 |
SCHEMBL ID | 82580 |
MeSH ID | M0380300 |
Synonym |
---|
tetrahydro-1,3-dimethyl-2(1h)pyrimidine |
brn 0110562 |
n,n'-dimethyltrimethyleneurea |
einecs 230-625-6 |
ccris 4322 |
tetrahydro-1,3-dimethyl-1h-pyrimidin-2-one |
dimethylpropyleneurea |
ec 230-625-6 |
dmpu |
7226-23-5 |
2(1h)-pyrimidinone, tetrahydro-1,3-dimethyl- |
2-pyrimidone,tetrahydro,1,3-dimethyl |
1,3-dimethyltetrahydropyrimidin-2(1h)-one |
inchi=1/c6h12n2o/c1-7-4-3-5-8(2)6(7)9/h3-5h2,1-2h |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone, 98% |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone, absolute, over molecular sieve (h2o <=0.03%), >=99.0% (gc) |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone |
CHEMBL12284 |
AKOS005145503 |
D2014 |
n,n'-dimethylpropyleneurea |
1,3-dimethyl-1,3-diazinan-2-one |
A837469 |
EN300-82368 |
1,3-dimethyl-3,4,5,6-tetrahydro-2[1h]-pyrimidinone |
n,n'-dimethylpropylene urea |
FT-0606689 |
SCHEMBL82580 |
J-503925 |
1,3-dimethyl-2-oxohexahydropyrimidine |
n,n'-dimethylproyleneurea |
1,3-dimethyl-3,4,5,6-tetrahydro-2 [1h]-pyrimidinone |
1,3-dimethyl-3,4,5,6-tetrahydropyrimidinone |
1,3-dimethyl-3,4,5,6tetrahydro-2(1h)-pyrimidinone |
1,3-dimethyl-tetrahydro-pyrimidin-2-one |
1,3-dimethyltetrahydro-2(1h)-pyrimidone |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidone |
1,3-dimethyl-3,4,5,6-tetrahydro-2 (1h)pyrimidinone |
1,3-dimethyl-3,4,5,6-tetrahydro-(1h)-pyrimidin-2-one |
1,3-di-methyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone |
1,3-dimethyltetrahydro-2(1h)pyrimidinon |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrirnidinone |
1,3-dimethyl-2,4,5,6-tetrahydro-2(1h)-pyrimidinone |
1,3-dimethyl-tetrahydro-2-1h-pyrimidinone |
1,3-dimethyltetrahydro-2-(1h)-pyrimidinone |
1,3-di- methyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone |
n,n'-dimethyl -1,4,5,6-tetrahydro-2-pyrimidone |
1,3-dimethyl-3,4,5,6-tetrahydro-2-(1h)-pyrimidinone |
1,3-dimethyl-3,4,5,6-tetrahydro 2(1h) pyrimidone |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinon |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)pyrimidinone |
1,3-dimethyl -3,4,5,6-tetrahydro-2(1h)-pyrimidinone |
1,3-dimethyl-3,4,5, 6-tetrahydro -2(1h)-pyrimidinone |
dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone |
n,n'-dimethyl-1,4,5,6-tetrahydro-2-pyrimidone |
1,3-dimethyl-3,4,5,6-tetrahydro-2 (1h)-pyrimidone |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)- pyrimidinone |
1,3-dimethyl tetrahydropyrimidin-2(1h)-one |
1,3-dimethyl-3,4,5,6-tetrahydro 2 (1h)-pyrimidinone |
1,3-dimethyl-3,4,5,6-tetrahydro-2 (1 h)-pyrimidinone |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1 h)-pyrimidinone |
1,3-dimethyl-3,4,5,6-tetrahydropyrimidin-2-one |
dimethylpropyl-eneurea |
1,3-dimethyl-3,4,5,6-tetrahydro-2-pyrimidinone |
1,3-dimethyl-tetrahydropyrimidin-2-one |
1,3-dimethyl-3,4,5,6-tetrahydro2(1h)-pyrimidinone |
1,3-dimethyltetrahydro-2-pyrimidinone |
1,3-dimethyltetrahydro-2(1h)-pyrimidinone |
1,3-dimethyl-3,4,5,6-tetrahydro- -2-(1h)-pyrimidone |
1,3-dim-ethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone |
1,3-dimethyl propylene urea |
1,3-dimethyl-3,4,5,6-tetrahydro-2 (1h)-pyrimidinone |
1,3-dimethyl-3,4,5,6-tetra-hydro-(1h)-pyrimidin-2-one |
n, n'-dimethylpropyleneurea |
1,3-dimethyl-tetrahydro -pyrimidin-2-one |
1,3-dimethyl-3,4,5,6-tetrahydro-2-(1h)pyrimidone |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)pyrimdinone |
1,3 dimethyl 3,4,5,6-tetrahydro-2-pyrimidone |
STR03401 |
tetrahydro-1,3-dimethyl-2(1h)pyrimidin-2-onee |
1,3-dimethyl-tetrahydro-2(1h)-pyrimidone |
mfcd00006550 |
DTXSID3074575 , |
CS-W009128 |
P17490 |
F0001-1844 |
BCP25854 |
labotest-bb lt00848352 dmpu dimethylpropylene urea dimethyl(1,3-)-3,4,5,6-tetrahydro-2h-pyrimidone 1,3-dimet |
Q416637 |
n,n-dimethyl-propylene-urea |
AMY12538 |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone (dmpu) |
SY002520 |
1,3-dimethyltetrahydro-2-pyrimidone |
n,n'-dimethylpropyleneurea (dmpu) |
PB47348 |
1,3-dimethyl-2-oxohexahydropyrimidine, n,n'-dimethylpropylene urea, dmpu |
1,3-dmethyl-3,4,5,6-tetrahydro-2(1h)-pyrimidinone |
Z1237078782 |
HY-Y0100 |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1570847 | Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay | 2019 | ACS medicinal chemistry letters, Oct-10, Volume: 10, Issue:10 | A Bioreductive Prodrug of Cucurbitacin B Significantly Inhibits Tumor Growth in the 4T1 Xenograft Mice Model. |
AID1570846 | Cytotoxicity against human MCF7 cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay | 2019 | ACS medicinal chemistry letters, Oct-10, Volume: 10, Issue:10 | A Bioreductive Prodrug of Cucurbitacin B Significantly Inhibits Tumor Growth in the 4T1 Xenograft Mice Model. |
AID71672 | Percent of untreated control cell growth evaluated in friend leukemia cells on day 3 at a concentration of 2 mM | 1981 | Journal of medicinal chemistry, Sep, Volume: 24, Issue:9 | Cyclic urea and thiourea derivatives as inducers of murine erythroleukemia differentiation. |
AID71653 | The degree of erythroid maturation was measured by assessing the proportion of benzidine-positive cells at a concentration of 2 mM | 1981 | Journal of medicinal chemistry, Sep, Volume: 24, Issue:9 | Cyclic urea and thiourea derivatives as inducers of murine erythroleukemia differentiation. |
AID71664 | Cell growth of friend erythroleukemia cells measured as percentage of control on day 6 at a concentration of 2 mM | 1981 | Journal of medicinal chemistry, Sep, Volume: 24, Issue:9 | Cyclic urea and thiourea derivatives as inducers of murine erythroleukemia differentiation. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 1 (10.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (40.00) | 29.6817 |
2010's | 5 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.32) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 11 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |