<<1--2,4-bis(diisopropylamino)-1,2-azaarseten-1-yl>triphenylphosphonium>-tetraphenylborat

Base Information

Chemical Name:<<1--2,4-bis(diisopropylamino)-1,2-azaarseten-1-yl>triphenylphosphonium>-tetraphenylborat
CAS No.:120312-26-7
Molecular Formula:C₂₄H₂₀B*C₃₈H₅₇As₂ClN₄P
Molecular Weight:1105.4
Hs Code.:

<<1-<Chlor(diisopropylamino)arsano>-2,4-bis(diisopropylamino)-1,2-azaarseten-1-yl>triphenylphosphonium>-tetraphenylborat

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Chemical Property of <<1--2,4-bis(diisopropylamino)-1,2-azaarseten-1-yl>triphenylphosphonium>-tetraphenylborat

Chemical Property:

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Technology Process of <<1--2,4-bis(diisopropylamino)-1,2-azaarseten-1-yl>triphenylphosphonium>-tetraphenylborat

There total 3 articles about <<1--2,4-bis(diisopropylamino)-1,2-azaarseten-1-yl>triphenylphosphonium>-tetraphenylborat 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: 84.0%

: 70908-30-4
Dichlor(diisopropylamino)arsan

: 143-66-8
sodium tetraphenyl borate

: 120312-28-9
Cyan(triphenylphosphoranyliden)methan

: 120312-26-7
<<1--2,4-bis(diisopropylamino)-1,2-azaarseten-1-yl>triphenylphosphonium>-tetraphenylborat

Guidance literature:: In tetrahydrofuran;

Reference yield:

: C₁₂H₂₈AsClN₂

: 120312-26-7
<<1--2,4-bis(diisopropylamino)-1,2-azaarseten-1-yl>triphenylphosphonium>-tetraphenylborat

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / toluene / -78 deg C to RT

2: 84 percent / tetrahydrofuran

In tetrahydrofuran; toluene;

Reference yield:

: 105663-75-0
Natrium-cyan(triphenylphosphoranyliden)methanid

: 120312-26-7
<<1--2,4-bis(diisopropylamino)-1,2-azaarseten-1-yl>triphenylphosphonium>-tetraphenylborat

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / toluene / -78 deg C to RT

2: 84 percent / tetrahydrofuran

In tetrahydrofuran; toluene;