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Merck
CN

357804

4′-碘苯乙酮

≥97%

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关于此项目

线性分子式:
IC6H4COCH3
化学文摘社编号:
分子量:
246.05
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
236-372-8
MDL number:
Assay:
≥97%
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Quality Level

assay

≥97%

mp

82-84 °C (lit.)

functional group

iodo, ketone

SMILES string

CC(C1=CC=C(I)C=C1)=O

InChI

1S/C8H7IO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3

InChI key

JZJWCDQGIPQBAO-UHFFFAOYSA-N

General description

已有研究报道了Pd(0)催化的4′-碘代苯乙酮与硅氧烷的交叉偶联反应。 已有研究报道了在流动反应器中由Pd纳米颗粒催化的4′-碘代苯乙酮与苯乙烯的Heck-Mizoroki反应。

Application

4′-碘代苯乙酮可用作钯催化的偶联反应的底物。 它可用于合成喹啉类潜在抗癌剂。


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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Klaas Mennecke et al.
Beilstein journal of organic chemistry, 5, 21-21 (2009-07-11)
The preparation of monolithic polyionic supports which serve as efficient heterogeneous supports for palladium(0) nanoparticles is described. These functionalized polymers were incorporated inside a flow reactor and employed in Suzuki-Miyaura and Heck cross couplings under continuous flow conditions.
S E Denmark et al.
Organic letters, 3(11), 1749-1752 (2001-06-19)
A sequential ring-closing metathesis/silicon-assisted cross-coupling sequence has been developed. Alkenyldimethylsilyl ethers of omega-unsaturated alcohols undergo facile ring closure with Schrock's catalyst to afford five-, six-, and seven-membered cycloalkenylsiloxanes bearing substituents on both alkenyl carbons. These siloxanes were highly effective coupling
Chemistry Letters (Jpn), 2049-2049 (1989)



全球贸易项目编号

货号GTIN
357804-5G04061831812688
357804-25G04061831812671