InH₃(C₃H₂N₂(C₉H₁₁)2)

Base Information

Chemical Name:InH₃(C₃H₂N₂(C₉H₁₁)2)
CAS No.:311311-56-5
Molecular Formula:C₂₁H₂₇InN₂
Molecular Weight:422.279
Hs Code.:

InH<sub>3</sub>(C<sub>3</sub>H<sub>2</sub>N<sub>2</sub>(C<sub>9</sub>H<sub>11</sub>)2)

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Chemical Property of InH₃(C₃H₂N₂(C₉H₁₁)2)

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Technology Process of InH₃(C₃H₂N₂(C₉H₁₁)2)

There total 3 articles about InH₃(C₃H₂N₂(C₉H₁₁)2) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

: 153594-82-2
trimethylamineindium trihydrate

: 141556-42-5
[1,3-bis(2,4,6-trimethylphenyl)imidazol]-2-ylidene

: 311311-56-5
InH₃(C₃H₂N₂(C₉H₁₁)2)

Guidance literature:: In water; ethylene glycol; other Radiation; Ir complex and ligand suspended in ethylene glycol, under purging N2 atm. suspn. subjected to reflux for 15 min in microwawe oven with frequencyof 2450 MHz, cooled to room temp., pptd. with satd. aq. soln. of KPF6; filtered, recrystd. from MeCN/Et2O;
DOI:10.1246/cl.2000.1206

Reference yield: 86.0%

: 128448-03-3
lithium tetrahydridoindanate

: 141556-42-5
[1,3-bis(2,4,6-trimethylphenyl)imidazol]-2-ylidene

: 311311-56-5
InH₃(C₃H₂N₂(C₉H₁₁)2)

Guidance literature:: In diethyl ether; stirred for 2 h at room temp.; solvent removed in vacuo, residue dissolved in toluene, filtd., storage for 24 h at -35°C, crystals sepd.; elem. anal.;
DOI:10.1021/om0004951

Reference yield: 65.0%

: 128448-03-3
lithium tetrahydridoindanate

: 593-81-7
trimethylamine hydrochloride

: 141556-42-5
[1,3-bis(2,4,6-trimethylphenyl)imidazol]-2-ylidene

: 311311-56-5
InH₃(C₃H₂N₂(C₉H₁₁)2)

: 311311-57-6
InH₂Cl(C₃H₂N₂(C₉H₁₁)2)

Guidance literature:: In diethyl ether; stirred for 2.5 h at -50°C, added C3H2N2(C9H11)2 and stirred for 2 h at -20°C; ppt. collected and recrystd. from toluene at -35°C;
DOI:10.1021/om0004951