7435-61-2

Basic information

• Product Name: 5-isobutyl-1,3-dimethylbarbituric acid
• Synonyms: 5-isobutyl-1,3-dimethylbarbituric acid;1,3-Dimethyl-5-(2-methylpropyl)-2,4,6(1H,3H,5H)-pyrimidinetrione;1,3-Dimethyl-5-isobutylpyrimidine-2,4,6(1H,3H,5H)-trione;Einecs 231-085-4
• CAS NO: 7435-61-2
• Molecular Formula: C10H16N2O3
• Molecular Weight: 212.24564
• EINECS: 231-085-4
• Mol File: 7435-61-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 282.2°C at 760 mmHg
• Flash Point: 109°C
• Appearance: /
• Density: 1.122g/cm³
• Vapor Pressure: 0.00341mmHg at 25°C
• Refractive Index: 1.482
• CAS DataBase Reference: 5-isobutyl-1,3-dimethylbarbituric acid(CAS DataBase Reference)
• NIST Chemistry Reference: 5-isobutyl-1,3-dimethylbarbituric acid(7435-61-2)
• EPA Substance Registry System: 5-isobutyl-1,3-dimethylbarbituric acid(7435-61-2)

Safety Data

• Hazardous Substances Data: 7435-61-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H16N2O3/c1-6(2)5-7-8(13)11(3)10(15)12(4)9(7)14/h6-7H,5H2,1-4H3

Upstream product

• 769-42-6 1,3-dimethylbarbituric acid 
• 78-83-1 2-methyl-propan-1-ol 
• 83814-08-8 1,3-dimethyl-5-(2-methylpropylidene)pyrimidine-2,4,6(1H,3H,5H)-trione 

Relevant articles and documents

Selective reduction of barbituric acids using SmI2/H 2O: Synthesis, reactivity, and structural analysis of tetrahedral adducts

Making a mark: Since the 1864 landmark discovery by Adolf von Baeyer, barbituric acids have played a prominent role in organic synthesis. Herein, the first chemoselective monoreduction of barbituric acids to the corresponding hemiaminals is described. The method delivers mono- and bicyclic hemiaminal products by a general single-electron-transfer polarity reversal mechanism. Re-use of this article is permitted in accordance with the Terms and Conditions set out at http://angewandte.org/open.