(4-bromo-5-(5-bromoselenophen-2-yl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)methanol

Base Information

Chemical Name:(4-bromo-5-(5-bromoselenophen-2-yl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)methanol
CAS No.:1003004-75-8
Molecular Formula:C₁₄H₈Br₂Cl₂N₂OSe
Molecular Weight:529.904
Hs Code.:

Synonyms:(4-bromo-5-(5-bromoselenophen-2-yl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)methanol

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Chemical Property of (4-bromo-5-(5-bromoselenophen-2-yl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)methanol

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Technology Process of (4-bromo-5-(5-bromoselenophen-2-yl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)methanol

There total 1 articles about (4-bromo-5-(5-bromoselenophen-2-yl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)methanol 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: 95.0%

: 1003004-69-0
4-bromo-5-(5-bromo-selenophen-2-yl)-1-(2,4-dichloro-phenyl)-1H-pyrazole-3-carboxylic acid ethyl ester

: 1003004-75-8
(4-bromo-5-(5-bromoselenophen-2-yl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)methanol

Guidance literature:: 4-bromo-5-(5-bromo-selenophen-2-yl)-1-(2,4-dichloro-phenyl)-1H-pyrazole-3-carboxylic acid ethyl ester; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 0.5h;

With water; In tetrahydrofuran;

Reference yield: 92.0%

: 1003004-75-8
(4-bromo-5-(5-bromoselenophen-2-yl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)methanol

: 124-63-0
methanesulfonyl chloride

: 1003004-76-9
methanesulfonic acid 4-bromo-5-(5-bromo-selenophen-2-yl)-1-(2,4-dichloro-phenyl)-1H-pyrazol-3-ylmethyl ester

Guidance literature:: (4-bromo-5-(5-bromoselenophen-2-yl)-1-(2,4-dichlorophenyl)-1H-pyrazol-3-yl)methanol; With triethylamine; In tetrahydrofuran; at 0 ℃; for 0.5h;

methanesulfonyl chloride; In tetrahydrofuran; at 20 ℃; for 8h;