62855-78-1

Basic information

• Product Name: 1,2-bis(thiocyanatomethyl)benzene
• Synonyms: 1,2-bis(thiocyanatomethyl)benzene
• CAS NO: 62855-78-1
• Molecular Weight: 220.319
• Mol File: 62855-78-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-bis(thiocyanatomethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-bis(thiocyanatomethyl)benzene(62855-78-1)
• EPA Substance Registry System: 1,2-bis(thiocyanatomethyl)benzene(62855-78-1)

Safety Data

• Hazardous Substances Data: 62855-78-1(Hazardous Substances Data)

Upstream product

• 333-20-0 potassium thioacyanate 
• 91-13-4 α,α'-dibromo-o-xylene 
• 612-12-4 o-Xylylene dichloride 

Downstream Products

• 3886-39-3 1,4-dihydrobenzo-2,3-dithiane 

Relevant articles and documents

Thiocyanation and 2-Amino-1,3-thiazole Formation in Water Using Recoverable and Reusable Glycosylated Resorcin[4]arene Cavitands

A family of three spatially directional resorcin[4]arene cavitand glycoconjugates (RCGs) have been applied as efficient recoverable and reusable inverse phase transfer catalysts for eco- A nd environmentally friendly thiocyanation and 2-amino-1,3-thiazole formation reactions in water. The results show that RCGs (1 mol %) were capable of hosting and catalyzing various water-insoluble bromo/thiocyanato substrates in water without the use of any co-organic solvents. The recoverability and reusability of RCG catalytic systems, that is, RCG1 and RCG3, were also examined upon a simple extraction of the desired products using DCM or ethyl acetate, followed by subjecting the recovered aqueous solution containing the RCG catalysts to the next reaction cycles.

Revisiting nucleophilic substitution reactions: Microwave-assisted synthesis of azides, thiocyanates, and sulfones in an aqueous medium

A practical, rapid, and efficient microwave (MW) promoted synthesis of various azides, thiocyanates, and sulfones is described in an aqueous medium. This general and expeditious MW-enhanced nucleophilic substitution approach uses easily accessible starting materials such as halides or tosylates in reaction with alkali azides, thiocyanates, or sulfinates in the absence of any phase-transfer catalyst, and a variety of reactive functional groups are tolerated.