N-(2,3-dibromopropyl)-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea

Base Information

Chemical Name:N-(2,3-dibromopropyl)-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea
CAS No.:118150-12-2
Molecular Formula:C₁₈H₂₁Br₂N₂O₂PS₂
Molecular Weight:552.291
Hs Code.:

Synonyms:N-(2,3-dibromopropyl)-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea

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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 N-(2,3-dibromopropyl)-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea

Chemical Property:

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Technology Process of N-(2,3-dibromopropyl)-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea

There total 3 articles about N-(2,3-dibromopropyl)-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea 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: 50.0%

: 129769-26-2
N-allyl-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea

: 118150-12-2
N-(2,3-dibromopropyl)-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea

Guidance literature:: With bromine; In chloroform; for 1h; Ambient temperature;

Reference yield:

: 22077-44-7
O,O-diphenyl phosphorochloridothioate

: 118150-12-2
N-(2,3-dibromopropyl)-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / triethylamine / CHCl₃ / 4 h / Ambient temperature

2: 50 percent / bromine / CHCl₃ / 1 h / Ambient temperature

With bromine; triethylamine; In chloroform;

Reference yield:

: 38069-31-7
N-allyl-S-ethylisothiourea hydrobromide

: 118150-12-2
N-(2,3-dibromopropyl)-N'-(diphenoxyphosphinothioyl)-S-ethylisothiourea

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / triethylamine / CHCl₃ / 4 h / Ambient temperature

2: 50 percent / bromine / CHCl₃ / 1 h / Ambient temperature

With bromine; triethylamine; In chloroform;