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Key Documents

215880

Sigma-Aldrich

醋酸锰(III) 二水合物

97%

同義詞:

Manganese triacetate dihydrate

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About This Item

線性公式:
(CH3COO)3Mn · 2H2O
CAS號碼:
分子量::
268.10
Beilstein:
3732626
EC號碼:
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.23

品質等級

化驗

97%

形狀

powder or chunks

反應適用性

core: manganese

SMILES 字串

O.O.CC(=O)O[Mn](OC(C)=O)OC(C)=O

InChI

1S/3C2H4O2.Mn.2H2O/c3*1-2(3)4;;;/h3*1H3,(H,3,4);;2*1H2/q;;;+3;;/p-3

InChI 密鑰

ONJSLAKTVIZUQS-UHFFFAOYSA-K

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一般說明

Manganese(III) acetate dihydrate is a coordination compound of manganese in the +3 oxidation state, exhibiting moderate solubility in water and acetic acid. It is used as a precursor for synthesizing manganese oxides and other manganese-containing materials. These materials have applications in batteries, catalysis, and other energy-related technologies. Additionally, it is also used as a mild and selective oxidizing agent in organic synthesis.

應用

Manganese(III) acetate dihydrate can be used as:      
  • A precursor in the synthesis of manganese oxide (Mn3O4) nanostructures, which are employed as anode materials in lithium-ion batteries.
  • A manganese source in the sol-gel synthesis of Mn-doped ZnO thin films. The incorporation of manganese ions into the ZnO lattice is essential for modifying the electronic and optical properties of the films.
  • A precursor for the synthesis of manganese oxide nanoparticles using a sol-gel process. These nanoparticles are evaluated for their performance in supercapacitor applications.     
  • A mild and selective oxidizing agent. Catalyzes allylic oxidation of a variety of alkenes in the presence of tert-butylhydroperoxide. Reagent used for radical cyclizations and α-keto-acetoxylation.

外觀

晶体学证据表明,该材料是 Mn (III) 的氧中心三角形,桥接乙酸盐的分子式为:Mn3O(OAc)9 · 6H2O。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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客戶也查看了

The Journal of Organic Chemistry, 62, 6978-6978 (1997)
Manganese(III)-Based Oxidative Free-Radical Cyclizations.
Barry B. Snider
Chemical reviews, 96(1), 339-364 (1996-02-01)
Demir, A.S. et al.
Tetrahedron, 55, 2441-2441 (1999)
Chemtracts Org. Chem., 403-403 (1991)
Tony K M Shing et al.
Organic letters, 8(14), 3149-3151 (2006-06-30)
Manganese(III) acetate catalyzed allylic oxidation of alkenes to the corresponding enones was investigated, showing excellent regioselectivity and chemoselectivity (functional group compatibility). Delta(5)-Steroids were transformed into bioactive Delta(5)-en-7-ones under a nitrogen atmosphere, whereas simple alkenes were converted into the corresponding enones

文章

Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis

Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis, and are some of the organic chemist’s most powerful tools for creating novel products. Below is a list of the most commonly used oxidizing and reducing agents currently available in our catalog.

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