84056-92-8

Basic information

• Product Name: N₃-cyclohexyl-N₁-(2-hydroxyethyl)-N₁-nitrosothiourea
• Synonyms: N₃-cyclohexyl-N₁-(2-hydroxyethyl)-N₁-nitrosothiourea
• CAS NO: 84056-92-8
• Molecular Weight: 231.319
• Mol File: 84056-92-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N₃-cyclohexyl-N₁-(2-hydroxyethyl)-N₁-nitrosothiourea(CAS DataBase Reference)
• NIST Chemistry Reference: N₃-cyclohexyl-N₁-(2-hydroxyethyl)-N₁-nitrosothiourea(84056-92-8)
• EPA Substance Registry System: N₃-cyclohexyl-N₁-(2-hydroxyethyl)-N₁-nitrosothiourea(84056-92-8)

Safety Data

• Hazardous Substances Data: 84056-92-8(Hazardous Substances Data)

Upstream product

• 1122-82-3 isothiocyanatocyclohexane 
• 81467-07-4 N-cyclohexyl-N'-(2-hydroxyethyl)thiourea 

Downstream Products

• 56242-66-1 2-(cyclohexylimino)thiazolidine 
• 80672-59-9 chlorhydrate de N-(thiazolin-2 yl-2) cyclohexylamine 
• 87191-81-9 2-(cyclohexylimino)-3-nitrosothiazolidine 
• 87191-82-0 2-hydroxyethyl-N-cyclohexylthionocarbamate 
• 87191-83-1 3-cyclohexyl-1-(2-chloroethyl)thiourea 
• 107-21-1 ethylene glycol 
• 75-07-0 acetaldehyde 
• 1122-82-3 isothiocyanatocyclohexane 
• 66929-45-1 3-cyclohexyl-1-(2-hydroxyethyl)-1-nitrosourea 
• 2387-23-7 1,3-Dicyclohexylurea 
• 13027-13-9 2-hydroxyethyl N-cyclohexylcarbamate 
• 66929-46-2 3-cyclohexyl-1-(2-hydroxyethyl) urea 
• 76310-06-0 2-(cyclohexylimino)-3-nitroso-2-oxazolidine 
• 10002-37-6 2-(cyclohexylamino)-2-oxazoline 

Relevant articles and documents

Synthesis of Novel N-Nitrosothioureas and Examination of Their Mechanisms of Formation by High-Field Nitrogen-15 and Carbon-13 Nuclear Magnetic Resonance Spectra of Specifically Labeled Compounds

An examination by 15N NMR of Na15NO2 under various conditions of acidity led to the identification of several electrophilic nitrogen species.This permitted the selection of reaction conditions of low acidity which favor nitrosation at the nitrogen atom of thioureas rather than on the normally more reactive sulfur, leading to the isolation of novel N-nitrosothioureas.In contrast it was shown by employing 15N and 13C labeling that higher acidity conditions favor reaction via a detectable thionitrosyl intermediate.