1,3-Divinyltetrahydro-1H-pyrimidin-2-one

Base Information

Chemical Name:1,3-Divinyltetrahydro-1H-pyrimidin-2-one
CAS No.:28084-37-9
Molecular Formula:C₉H₈O
Molecular Weight:132.162
Hs Code.:
European Community (EC) Number:248-826-2
DSSTox Substance ID:DTXSID10182361
Nikkaji Number:J250.648C
Wikidata:Q83053025
Mol file:28084-37-9.mol

Synonyms:1,3-Divinyltetrahydro-1H-pyrimidin-2-one;28084-37-9;1,3-bis(ethenyl)-1,3-diazinan-2-one;EINECS 248-826-2;SCHEMBL4590154;DTXSID10182361;1,3-Diethenyltetrahydropyrimidin-2(1H)-one;FT-0727001

Suppliers and Price of 1,3-Divinyltetrahydro-1H-pyrimidin-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 6 raw suppliers

Chemical Property of 1,3-Divinyltetrahydro-1H-pyrimidin-2-one

Chemical Property:

Vapor Pressure:0.107mmHg at 25°C
Boiling Point:221.5°Cat760mmHg
Flash Point:84.1°C
PSA：23.55000
Density:1.2g/cm³
LogP:1.27690
XLogP3:0.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:152.094963011
Heavy Atom Count:11
Complexity:171

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CN1CCCN(C1=O)C=C
General Description 1,3-Divinyltetrahydro-1H-pyrimidin-2-one is a heterocyclic compound featuring a saturated pyrimidinone core substituted with vinyl groups at the 1 and 3 positions. It is also referred to as N,N'-divinylpropyleneurea, highlighting its structural relationship to propyleneurea. 1,3-divinyltetrahydro-1H-pyrimidin-2-one is of interest in synthetic chemistry, particularly as a monomer or intermediate in polymerization reactions due to its reactive vinyl groups. Its hexahydropyrimidin-2-one scaffold contributes to its potential utility in designing functional materials or bioactive molecules. The presence of the divinyl moiety allows for further chemical modifications, making it a versatile building block in organic synthesis.

Technology Process of 1,3-Divinyltetrahydro-1H-pyrimidin-2-one

There total 129 articles about 1,3-Divinyltetrahydro-1H-pyrimidin-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%

: 271-89-6
1-benzofurane

: 74-88-4
methyl iodide

: 4265-25-2
2-methylbenzofuran

Guidance literature:: 1-benzofurane; With tert.-butyl lithium; In tetrahydrofuran; hexane; at -78 ℃; for 2h; Inert atmosphere;

methyl iodide; In tetrahydrofuran; hexane; at -78 - 20 ℃; Inert atmosphere;
DOI:10.1002/anie.201107811

Reference yield: 95.0%

: 1745-81-9
o-Allylphenol

: 4265-25-2
2-methylbenzofuran

Guidance literature:: With copper diacetate; palladium dichloride; In N,N-dimethyl-formamide; at 100 ℃; for 1h;
DOI:10.1016/S0022-328X(98)00415-X