Se-4-chlorophenyl benzeneselenoate

Base Information

Chemical Name:Se-4-chlorophenyl benzeneselenoate
CAS No.:94706-41-9
Molecular Formula:C₁₃H₉ClOSe
Molecular Weight:295.627
Hs Code.:

Synonyms:Se-4-chlorophenyl benzeneselenoate

Suppliers and Price of Se-4-chlorophenyl benzeneselenoate

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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 Se-4-chlorophenyl benzeneselenoate

Chemical Property:

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Technology Process of Se-4-chlorophenyl benzeneselenoate

There total 4 articles about Se-4-chlorophenyl benzeneselenoate 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: 90.0%

: 20541-49-5
bis(p-chlorophenyl) diselenide

: 98-88-4
benzoyl chloride

: 94706-41-9
Se-4-chlorophenyl benzeneselenoate

Guidance literature:: With indium; In dichloromethane; for 12h; Inert atmosphere; Reflux;
DOI:10.1016/j.tet.2009.03.069

Reference yield: 86.0%

: 20541-49-5
bis(p-chlorophenyl) diselenide

: 93-97-0
benzoic acid anhydride

: 94706-41-9
Se-4-chlorophenyl benzeneselenoate

Guidance literature:: With C₄₀H₃₂N₄O₇Ti₂⁽²⁺⁾*2C₈F₁₇O₃S^(1-); zinc; In 1,2-dichloro-ethane; at 25 ℃; for 5h;

Reference yield:

: 637-87-6
1-Chloro-4-iodobenzene

: 94706-41-9
Se-4-chlorophenyl benzeneselenoate

Guidance literature:: Multi-step reaction with 2 steps

1: selenium; copper(II) oxide; potassium hydroxide / dimethyl sulfoxide / 90 °C / Inert atmosphere

2: iron(III) chloride; dibenzoyl peroxide / dichloromethane / 3 h / 20 °C

With iron(III) chloride; selenium; copper(II) oxide; potassium hydroxide; dibenzoyl peroxide; In dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.tet.2019.130624