42877-24-7

Basic information

• Product Name: Thiocyanic acid, 1-phenyl-1,2-ethanediyl ester
• Synonyms: Styroldirhodanid;Phenyl-aethandiyl-bis-thiocyanat;Thiocyanic acid,1-phenyl-1,2-ethanediyl ester;phenyl-ethanediyl-bis thiocyanate;1.2-Dirhodan-1-phenyl-aethan
• CAS NO: 42877-24-7
• Molecular Formula: C10H8N2S2
• Molecular Weight: 220.319
• Mol File: 42877-24-7.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Thiocyanic acid, 1-phenyl-1,2-ethanediyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Thiocyanic acid, 1-phenyl-1,2-ethanediyl ester(42877-24-7)
• EPA Substance Registry System: Thiocyanic acid, 1-phenyl-1,2-ethanediyl ester(42877-24-7)

Safety Data

• Hazardous Substances Data: 42877-24-7(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 29284-59-1 thiocyanogen bromide 
• 1147550-11-5 ammonium thiocyanate 
• 302-04-5 Thiocyanate 
• 2290-65-5 trimethylsilyl isothiocyanate 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 333-20-0 potassium thioacyanate 
• 3535-84-0 thallium(I) thiocyanate 
• 505-14-6 thiocyanogen 
• 64-19-7 acetic acid 
• 96-09-3 styrene oxide 

Downstream Products

• 62-23-7 4-nitro-benzoic acid 
• 88734-63-8 7-Chlor-2-(2-phenyl-2-thiocyanatoethylthio)-4H,5H-pyrano<3,4-e><1,3>oxazin-4,5-dion 

Relevant articles and documents

A very efficient Cerium (IV) ammonium nitrate (CAN) mediated thiocyanation of aralkenes: Formation of dithiocyanates

A facile dithiocyanation of aralkenes mediated by Cerium (IV) ammonium nitrate is described.

One-pot anodic thiocyanation and isothiocyanation of alkenes

The one-pot anodic thiocyanation and isothiocyanation of alkenes in both acidic two-phase (water-dichloromethane) and homogeneous one-phase (water-acetonitrile) media has been studied. Optimisation experiments on tetramethylethylene as a model alkene invo

Ferric(III) chloride-promoted efficient thiocyanation of arylalkenes: A facile synthesis of dithiocyanates

Anhydrous FeCl3 oxidizes potassium thiocyanate to the corresponding radical and promotes subsequent addition to nucleophilic olefins to produce dithiocyanate derivatives under mild conditions with high efficiency. Excellent yields and chemosele