24966-93-6

Basic information

• Product Name: 4,4,6-trimethyl-2-(methylsulfanyl)-1,4-dihydropyrimidine hydroiodide (1:1)
• CAS NO: 24966-93-6
• Molecular Formula: C₈H₁₅IN₂S
• Molecular Weight: 298.1876
• Mol File: 24966-93-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 235.7°C at 760 mmHg
• Flash Point: 96.3°C
• Vapor Pressure: 0.0494mmHg at 25°C
• CAS DataBase Reference: 4,4,6-trimethyl-2-(methylsulfanyl)-1,4-dihydropyrimidine hydroiodide (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4,6-trimethyl-2-(methylsulfanyl)-1,4-dihydropyrimidine hydroiodide (1:1)(24966-93-6)
• EPA Substance Registry System: 4,4,6-trimethyl-2-(methylsulfanyl)-1,4-dihydropyrimidine hydroiodide (1:1)(24966-93-6)

Safety Data

• Hazardous Substances Data: 24966-93-6(Hazardous Substances Data)

Upstream product

• 5392-23-4 3,4-dihydro-4,4,6-trimethylpyrimidine-2(1H)-thione 
• 74-88-4 methyl iodide 

Downstream Products

• 4628-47-1 4,4,6-trimethyl-1,4-dihydropyrimidine-2(3H)-one 

Relevant articles and documents

The Reactions of Monosubstituted Guanidins with α,β-Unsaturated Ketones

Action of methyl-, benzyl- and phenylguanidine on mesityloxide yields the 2-R3-imino-4,4,6-trimethyl-1,2,3,4-tetrahydropyrimidines resp. 2-R3-aminopyrimidines 8b, c and e, cyclohexylidenacetone reacts with benzylguanidine to give the 2-benzylimino-4-methyl-1,3-diazaspiroundeca-4-en resp. the benzylaminodiazaspiroundecadien (8d).The isomeric 1- and 3-R3-pyrimidinimines (resp. -amines) 9 b-e and 10 b-e are not formed in the reaction.The structures were proved by spectroscopical and chemical methods. - Keywords: Guanidines, monosubstituted; Ketone, α,β-unsatturated; Pyrimidines, 2-alkylimino-1,2,3,4-tetrahydro