5-Isopentyl-5-methylbarbituric acid

Base Information

Chemical Name:5-Isopentyl-5-methylbarbituric acid
CAS No.:67051-30-3
Molecular Formula:C10H16N2O3
Molecular Weight:0
Hs Code.:
Mol file:67051-30-3.mol

Synonyms:5-Isopentyl-5-methyl-barbitursaeure;5-isopentyl-5-methyl-barbituric acid;BARBITURIC ACID,5-ISOPENTYL-5-METHYL;5-methyl-5-(3-methylbutyl) barbituric acid;2,6(1H,3H,5H)-Pyrimidinetrione,5-methyl-5-(3-methylbutyl);

Suppliers and Price of 5-Isopentyl-5-methylbarbituric acid

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 5 raw suppliers

Chemical Property of 5-Isopentyl-5-methylbarbituric acid

Chemical Property:

PSA：75.27000
Density:1.094g/cm³
LogP:1.45250

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of 5-Isopentyl-5-methylbarbituric acid

There total 2 articles about 5-Isopentyl-5-methylbarbituric acid 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: 70.0%

: 121823-85-6
diethyl 2-isopentyl-2-methylmalonate

: 57-13-6
urea

: 67051-30-3
5-methyl-5-(3-methylbutyl) barbituric acid

Guidance literature:: DOI:10.1016/0223-5234(88)90139-0

Reference yield:

: 57-13-6
urea

: 67051-30-3
5-methyl-5-(3-methylbutyl) barbituric acid

Guidance literature:: With sodium ethanolate;

Reference yield:

: 67051-30-3
5-methyl-5-(3-methylbutyl) barbituric acid

: 66843-01-4
acide (methyl-3 butene-2 yl)-5 methyl-5 barbiturique

Guidance literature:: Multi-step reaction with 2 steps

1: 20 percent / CrO₃/AcOH / 12 h / 20 °C

2: 100 percent / 95percent CH₃COOH

With chromium(VI) oxide; acetic acid;
DOI:10.1016/0223-5234(88)90139-0