1,3,2,4-Diazadiphosphetidine, 2,2,4,4-tetrafluoro-2,2,4,4-tetrahydro-1,3-dimethyl-2,4-bis(4-methylphen oxy)-

Base Information

Chemical Name:1,3,2,4-Diazadiphosphetidine, 2,2,4,4-tetrafluoro-2,2,4,4-tetrahydro-1,3-dimethyl-2,4-bis(4-methylphen oxy)-
CAS No.:94445-96-2
Molecular Formula:C₁₆H₂₀F₄N₂O₂P₂
Molecular Weight:410.288
Hs Code.:

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1,3,2,4-Diazadiphosphetidine, 2,2,4,4-tetrafluoro-2,2,4,4-tetrahydro-1,3-dimethyl-2,4-bis(4-methylphen oxy)-

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Technology Process of 1,3,2,4-Diazadiphosphetidine, 2,2,4,4-tetrafluoro-2,2,4,4-tetrahydro-1,3-dimethyl-2,4-bis(4-methylphen oxy)-

There total 2 articles about 1,3,2,4-Diazadiphosphetidine, 2,2,4,4-tetrafluoro-2,2,4,4-tetrahydro-1,3-dimethyl-2,4-bis(4-methylphen oxy)- 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:

: 106-44-5
p-cresol

: 3880-04-4
2,2,2,4,4,4-hexafluoro-1,3-dimethyl-1,3,2λ⁵,4λ⁵-diazadiphosphetidine

: 94445-96-2
2,2,4,4-Tetrafluoro-1,3-dimethyl-2,4-bis-p-tolyloxy-2λ⁵,4λ⁵-[1,3,2,4]diazadiphosphetidine

Guidance literature:: With n-butyllithium; Yield given. Multistep reaction; 1.) diethyl ether, hexane, 2 h, reflux, 2.) 4 h, reflux;
DOI:10.1007/BF00798756

Reference yield:

: 106-44-5
p-cresol

: 3880-04-4
2,2,2,4,4,4-hexafluoro-1,3-dimethyl-1,3,2λ⁵,4λ⁵-diazadiphosphetidine

: 94446-25-0
2,2,2,4,4-Pentafluoro-1,3-dimethyl-4-p-tolyloxy-2λ⁵,4λ⁵-[1,3,2,4]diazadiphosphetidine

: 94445-96-2
2,2,4,4-Tetrafluoro-1,3-dimethyl-2,4-bis-p-tolyloxy-2λ⁵,4λ⁵-[1,3,2,4]diazadiphosphetidine

Guidance literature:: With n-butyllithium; Yield given. Multistep reaction; 1.) diethyl ether, hexane, 30 min, reflux, 2.) 1 h, reflux;
DOI:10.1007/BF00798756