60211-89-4

Basic information

• Product Name: Cyclohexane, 1-iodo-2-isothiocyanato-, trans-
• CAS NO: 60211-89-4
• Molecular Formula: C7H10INS
• Molecular Weight: 267.134
• Mol File: 60211-89-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cyclohexane, 1-iodo-2-isothiocyanato-, trans-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexane, 1-iodo-2-isothiocyanato-, trans-(60211-89-4)
• EPA Substance Registry System: Cyclohexane, 1-iodo-2-isothiocyanato-, trans-(60211-89-4)

Safety Data

• Hazardous Substances Data: 60211-89-4(Hazardous Substances Data)

Upstream product

• 333-20-0 potassium thioacyanate 
• 110-83-8 cyclohexene 
• 60211-89-4 trans-1-iodo-2-isothiocyanatocyclohexane 
• 2010-58-4 iodine thiocyanate 
• 505-14-6 thiocyanogen 
• 3535-84-0 thallium(I) thiocyanate 

Downstream Products

• 77469-31-9 N-(trans-2-iodocyclohexyl)cyanothioformamide 
• 77469-20-6 (chloromethylthio)cyano-N-(trans-2-iodocyclohexyl)methanimine 
• 77469-28-4 2-butyl-cis-3a,4,5,6,7,7a-hexahydrobenzothiazole 
• 60211-89-4 cis-1-iodo-2-isothiocyanatocyclohexane 
• 77469-36-4 N-(trans-2-iodocyclohexyl)thiobenzamide 
• 77469-34-2 N-(trans-2-iodocyclohexyl)ethynylthioformamide 
• 77469-29-5 phenyl-2 cis hexahydro 3a,4,5,6,7,7a benzothiazole 
• 77469-30-8 1-chloro-1-(4-methoxyphenyl)-2-(cis-3a,4,5,6,7,7a-hexahydrobenzothiazol-2-yl)ethylene 
• 77469-23-9 1-(4-methoxyphenyl)-2-(cis-3a,4,5,6,7,7a-hexahydrobenzothiazol-2-yl)acetylene 
• 77469-24-0 1-(cis-3a,4,5,6,7,7a-hexahydrobenzothiazol-2-yl)-2-phenylacetylene 
• 286-28-2 cyclohexene sulfide 
• 77469-33-1 N-(trans-2-iodocyclohexyl)(phenylethynyl)thioformamide 
• 77469-35-3 N-(trans-2-iodocyclohexyl)(trimethylsilylethynyl)thioformamide 
• 77469-32-0 N-(trans-2-iodocyclohexyl)-(4-methoxyphenylethynyl)thioformamide 

Relevant articles and documents

vic-Iodothiocyanates and Iodoisothiocyanates. Part 8. Addition of Iodine-Thiocyanogen to Alkenes under Ionic and Radical Conditions

Addition of iodine-thiocyanogen to alkenes in the dark proceeds by a regioselective ionic reaction to give mainly vic-iodoisothiocyanates, and under irradiation with u.v. light by a radical reaction to give mainly vic-iodothiocyanates.However, in the case of 1-methylene-4-t-butylcyclohexane even under irradiation by u.v. light, ionic addition of the reagent competes successfully with, and almost to the exclusion of, the radical pathway.

vic-Iodothiocyanates and Iodoisothiocyanates. Part 4. The Synthesis of 2-Substituted-2-thiazolines

The reactions of trans-1-iodo-2-isothiocyanatocyclohexane with a number of carbon nucleophiles to form 2-substituted-2-thiazolines are described.Reactions of several vic-iodoisothiocyanates with butil-lithium give products which are dependent on the solvent and/or temperature.