106456-85-3

Basic information

• Product Name: 4-(1,3-DITHIOLAN-2-YL)BENZONITRILE
• Synonyms: 4-(1,3-DITHIOLAN-2-YL)BENZONITRILE
• CAS NO: 106456-85-3
• Molecular Formula: C₁₀H₉NS₂
• Molecular Weight: 0
• Mol File: 106456-85-3.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(1,3-DITHIOLAN-2-YL)BENZONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1,3-DITHIOLAN-2-YL)BENZONITRILE(106456-85-3)
• EPA Substance Registry System: 4-(1,3-DITHIOLAN-2-YL)BENZONITRILE(106456-85-3)

Safety Data

• Hazardous Substances Data: 106456-85-3(Hazardous Substances Data)

Upstream product

• 619-65-8 4-cyanobenzoic Acid 
• 540-63-6 ethane-1,2-dithiol 
• 127732-82-5 4-(1,3-oxathiolan-2-yl)benzonitrile 
• 105-07-7 4-cyanobenzaldehyde 

Downstream Products

• 7153-22-2 ethyl 4-cyanobenzoate 
• 105-07-7 4-cyanobenzaldehyde 
• 78784-21-1 4-[1,3]dithiolan-2-yl-benzaldehyde 

Relevant articles and documents

Thioacetalization of carbonyl compounds by zeolite HSZ-360 as a new, effective heterogeneous catalyst

Thioacetal can be efficiently obtained at room temperature by simply dissolving the appropriate carbonyl compounds and 1,2-ethanedithiol, in dichloromethane, with zeolite HSZ-360 as a new heterogeneous catalyst. Satisfactory to good yields are obtained ev

Iron(III) fluoride: A highly efficient and versatile catalyst for the protection of carbonyl compounds under solvent-free conditions

Carbonyl compounds are successfully converted into oxathioacetals and dithioacetals with 2-mercaptoethanol and ethane-1,2-dithiol using a catalytic amount of iron(m) fluoride under solvent-free conditions. The catalysts were recovered and reused in variou

Indium-Catalyzed Reductive Dithioacetalization of Carboxylic Acids with Dithiols: Scope, Limitations, and Application to Oxidative Desulfurization

In this study an InI3-TMDS (1,1,3,3-tetramethyldisiloxane) reducing system effectively catalyzed the reductive dithioacetalization of a variety of aromatic and aliphatic carboxylic acids with 1,2-ethanedithiol or 1,3-propanedithiol leading to the one-pot preparation of either 1,3-dithiolane derivatives or a 1,3-dithiane derivative. Also, the intact indium catalyst continuously catalyzed the subsequent oxidative desulfurization of an in situ formed 1,3-dithiolane derivative, which led to the preparation of the corresponding aldehydes.

Silica-supported phosphorus pentoxide: A reusable catalyst for S,S-acetalization of carbonyl groups under ambient conditions

Phosphorus pentoxide supported on silica gel (P2O 5/SiO2) efficiently acts as a highly active and reusable catalyst for cyclic and non-cyclic S,S-acetalization of a variety of carbonyl compounds under mild, solvent-free an