28907-20-2

Basic information

• Product Name: 1,2-Cyclohexanedicarbonitrile, (1R,2S)-rel-
• CAS NO: 28907-20-2
• Molecular Formula: C8H10N2
• Molecular Weight: 134.181
• Mol File: 28907-20-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,2-Cyclohexanedicarbonitrile, (1R,2S)-rel-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Cyclohexanedicarbonitrile, (1R,2S)-rel-(28907-20-2)
• EPA Substance Registry System: 1,2-Cyclohexanedicarbonitrile, (1R,2S)-rel-(28907-20-2)

Safety Data

• Hazardous Substances Data: 28907-20-2(Hazardous Substances Data)

Upstream product

• 7429-37-0 trans-1,2-dibromocyclohexane 
• 143-33-9 sodium cyanide 
• 151-50-8 potassium cyanide 
• 68843-17-4 1,2-bis(5-thianthreniumyl)cyclohexane diperchlorate 
• 19246-38-9 cis-1,2-dibromocyclohexane 
• 1855-63-6 cyclohex-1-enecarbonitrile 
• 75-44-5 phosgene 
• 70925-10-9 cyclohexane-1,2-dicarboxamide 

Downstream Products

• 70925-19-8 trans-1,2-dicyanocyclohexane 
• 610-09-3 (1R,2S)-cyclohexane-1,2-dicarboxylic acid 
• 207518-98-7 cis-Cyclohexan-dicarbonsaeure-1,2-monoamid 

Relevant articles and documents

Ion Radicals. 46. Reactions of the Adducts of Thianthrene and Phenoxathiin Cation Radicals and Cyclohexene with Nucleophiles

Thianthrene cation radical perchlorate 1a reacts with cyclohexene to give an adduct .Reactions of 2a with CN-, C6H5S-, and I- have been studied in dimethyl sulfoxide (Me2SO) and ethanol at room temperature.Reaction of the analogous adduct of cyclohexene and phenoxathiin cation radical perchlorate 2b with I- in ethanol was also studied.The reactions indicate that the adducts have the trans-1,2 structure and undergo facile substitution (SN2) and subsequent elimination (E2) reactions at room temperature.