23356-03-8

Upstream product

• 931-51-1 cyclohexylmagnesiumchloride 

Downstream Products

• 24379-25-7 dichloro-tricyclohexyl-arsorane 
• 17729-76-9 tricyclohexyl-methyl-arsonium; iodide 
• 75465-80-4 Tricyclohexyliminoarsoran 
• 133102-12-2 (C₆H₁₁)3AsO*SO₃ 
• 25934-56-9 (CO)5Cr*As(C₆H₁₁)3=(CO)5CrAs(C₆H₁₁)3 
• 25921-53-3 (CO)3Fe(As(C₆H₁₁-cyclo)3)2 
• 91019-19-1 Cu((C₆H₁₁)3As)2ClO₄ 
• 90939-07-4 Zn((C₆H₁₁)3As)2ClO₄⁽¹⁺⁾*ClO₄^(1-)={Zn((C₆H₁₁)3As)2ClO₄}ClO₄ 
• 91019-14-6 Cd((C₆H₁₁)3As)2ClO₄⁽¹⁺⁾*ClO₄^(1-)={Cd((C₆H₁₁)3As)2ClO₄}ClO₄ 
• 90938-99-1 [Ag(OClO₃)(As(C₆H₁₁)3)2] 
• 79132-17-5 Hg(As(C₆H₁₁)3)2(OClO₃)⁽¹⁺⁾*ClO₄^(1-)=[Hg(As(C₆H₁₁)3)2(ClO₄)]ClO₄ 
• 210483-17-3 [Ag(NCO)(As(C₆H₁₁)3)2] 

Relevant academic research and scientific papers

Fundamental Study on Arsenic(III) Halides (AsX3; X = Br, I) toward the Construction of C3-Symmetrical Monodentate Arsenic Ligands

Arsenic ligands have attracted considerable attention in coordination chemistry. Arsenic(III) halides are the most important starting materials in the preparation of monodentate arsenic ligands. In this work, we optimized the synthetic methodologies of arsenic(III) halides (AsX3; X = Br, I) and examined the difference of their physical properties such as solubility to organic solvent and reactivity to nucleophiles. In addition, a wide variety of monodentate arsenic ligands were prepared with the obtained AsX3. Finally, the obtained monodentate arsenic ligands were utilized for copper-free Sonogashira cross-coupling reaction in the reaction system with porphyrin. The results showed that monodentate arsenic ligands have higher catalytic activity compared with triphenylphosphine because of the difference of the electronic features of lone pairs between arsenic and phosphorus atoms.

Tertiary arsine ligands for the Stille coupling reaction

The Stille coupling reaction is one of the most important coupling reactions. It is well known that the triphenylarsine ligand can accelerate the reaction rate of Stille coupling. However, other arsine ligands have never been investigated for the Stille c

Selective formation of ethanol from methanol, hydrogen and carbon monoxide

A process for the selective formation of ethanol which comprises contacting methanol, hydrogen and carbon monoxide with a catalyst system comprising cobalt acetylacetonate, a tertiary organo Group V A compound of the periodic Table, a first promoter comprising an iodine compound and a second promoter comprising a ruthenium compound.