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Merck
CN

905925

[Pd(terpy)(2-Cl-phen)](BF4)2

≥95%, powder or crystals

别名:

Ritter fluorination catalyst

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关于此项目

经验公式(希尔记法):
C27H18B2ClF8N5Pd
化学文摘社编号:
分子量:
727.95
MDL number:
UNSPSC Code:
12161600
NACRES:
NA.22
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产品名称

[Pd(terpy)(2-Cl-phen)](BF4)2 , ≥95%

assay

≥95%

form

powder or crystals

reaction suitability

core: palladium, reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: catalyst

mp

>300 °C

storage temp.

2-8°C

SMILES string

ClC(C=C1)=NC2=C1C=CC3=CC=C[N]([Pd]45[N]6=C(C7=CC=CC=[N]75)C=CC=C6C8=CC=CC=[N]84)=C32

Application

[Pd(terpy)(2-Cl-phen)](BF4)2 was developed in the Ritter lab for the elecrophilic fluorination of arenes.
Automate your fluorination reactions with Synple Automated Synthesis Platform (SYNPLE-SC002)

Legal Information

This product is manufactured pursuant to a license with Studiengesellschaft Kohle mbH (US Patent Pending 16/083,160 and PCT/US2017/021563).


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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分析证书(COA)

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Kumiko Yamamoto et al.
Nature, 554(7693), 511-514 (2018-02-23)
Aryl fluorides are widely used in the pharmaceutical and agrochemical industries, and recent advances have enabled their synthesis through the conversion of various functional groups. However, there is a lack of general methods for direct aromatic carbon-hydrogen (C-H) fluorination. Conventional