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Merck
CN

514365

乙酰丙酮酸铜

≥99.9% trace metals basis

别名:

2,4-戊二酮 铜(II) 衍生物, 2,4-戊二酮铜(II), Cu(acac)2, 乙酰丙酮铜

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关于此项目

线性分子式:
Cu(C5H7O2)2
化学文摘社编号:
分子量:
261.76
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
236-477-9
Beilstein/REAXYS Number:
4157957
MDL number:
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产品名称

乙酰丙酮酸铜, ≥99.9% trace metals basis

InChI key

QYJPSWYYEKYVEJ-FDGPNNRMSA-L

InChI

1S/2C5H8O2.Cu/c2*1-4(6)3-5(2)7;/h2*3,6H,1-2H3;/q;;+2/p-2/b2*4-3-;

SMILES string

CC(=O)\C=C(\C)O[Cu]O\C(C)=C/C(C)=O

assay

≥99.9% trace metals basis

form

powder

reaction suitability

core: copper

mp

284-288 °C (dec.) (lit.)

Quality Level

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Application

乙酰丙酮铜(II)可用作:
  • 用于全氧化物光电池中氧化铜原子层沉积的前体。
  • 苯乙烯的氮丙啶化(aziridination) 催化剂。
  • Huisgen-Click反应合成1,2,3-三唑的催化剂。

General description

乙酰丙酮铜(II)是一种有机金属配位化合物,广泛用作多种有机反应(包括氧化、交叉偶联和聚合反应)的催化剂。它也是制造有机金属框架(MOF)和纳米材料的前体。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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


历史批次信息供参考:

分析证书(COA)

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Atomic layer deposition of copper oxide using copper (II) acetylacetonate and ozone
Mari Endresen Alnes, et al.
Chem. Vap. Deposition, 18, 173-178 (2012)
Copper(II) acetylacetonate anchored onto an activated carbon as a heterogeneous catalyst for the aziridination of styrene
Ana Rosa Silva, et al.
Catalysis Today, 102-103, 154-159 (2005)
David N Paglia et al.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 30(12), 1971-1978 (2012-06-02)
This study quantified the effects of local intramedullary delivery of an organic vanadium salt, which may act as an insulin-mimetic on fracture healing. Using a BB Wistar rat femoral fracture model, local vanadyl acetylacetonate (VAC) was delivered to the fracture
Yanfang Li et al.
Dalton transactions (Cambridge, England : 2003), 41(13), 3807-3816 (2012-02-24)
Biscyclometalated iridium(III) complexes with an ancillary acetylacetone ligand, Ir(L)(2)(acac), (L = 2-(benzo[b]thiophen-2-yl)pyridine (btp), 1-phenylisoquinoline (piq), 2-phenylbenzothiazole (bt), 2-phenylpyridine (ppy), acac = deprotonated acetylacetone), demonstrate spectroscopic changes in their UV-Vis absorption and luminescent emission under acidic conditions. Such changes were found
Ik-Soo Shin et al.
The Analyst, 136(10), 2151-2155 (2011-03-25)
Though recently Ir(III) complexes have attracted much interest in electrochemiluminescent (ECL) analysis due to their high emission in various wavelengths, there were a few studies reported on its analytical applications. In this study, we evaluate the ECL from (pq)(2)Ir(acac) (pq

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