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267953

Sigma-Aldrich

铁

powder, <10 μm, ≥99.9% trace metals basis

同義詞:

Fe

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About This Item

線性公式:
Fe
CAS號碼:
7439-89-6
分子量：:
55.85
EC號碼:
231-096-4
MDL號碼:
MFCD00010999
分類程式碼代碼:
12161600
PubChem物質ID:
24856253
NACRES:
NA.22

化驗

≥99.9% trace metals basis

形狀

powder

反應適用性

core: iron
reagent type: catalyst

電阻係數

9.71 μΩ-cm

粒徑

<10 μm

bp

2750 °C (lit.)

mp

1535 °C (lit.)

密度

7.86 g/mL at 25 °C (lit.)

SMILES 字串

[Fe]

InChI

1S/Fe

InChI 密鑰

XEEYBQQBJWHFJM-UHFFFAOYSA-N

相關類別

應用

Iron powder is commonly used as the catalyst for a wide variety of organic transformations. Applications include:
  • Reduction of nitroaromatic compounds to aromatic amines.
  • Iron-mediated polymerization of methyl methacrylate (MMA) in the presence of a reversible addition-fragmentation chain transfer (RAFT) agent, 2-cyanoprop-2-yl 1-dithionaphthalate (CPDN).
  • Synthesis of pyrrolo[1,2-a]quinoxaline derivatives.
  • Conversion of ketoximes to the corresponding ketones by treatment with iron powder.
  • Iron-catalyzed cross-coupling reaction of imidazoles with vinyl bromides and vinyl chlorides.

象形圖

Flame
GHS02

訊號詞

Warning

危險聲明

H228,H252

危險分類

Flam. Sol. 2 - Self-heat. 2

儲存類別代碼

4.2 - Pyrophoric and self-heating hazardous materials

水污染物質分類（WGK）

nwg

閃點（°F）

69.8 °F

閃點（°C）

21 °C

個人防護裝備

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

分析證明 (COA)

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铁

Krafft, M. E.; Holton, R. A.
Journal of the American Chemical Society, 106, 7619-7619 (1984)
Ito, S.; Inoue, K.; Mastumoto, M.
Journal of the American Chemical Society, 104, 6450-6450 (1982)
Iron?Catalyzed Cross?Coupling Reaction of Vinyl Bromides or Chlorides with Imidazoles in the Absence of Ligands and Additives.
Mao J, et al.
Advanced Synthesis & Catalysis, 351(9), 1268-1272 (2009)
Reduction of nitroarenes to aromatic amines with nanosized activated metallic iron powder in water.
Wang L, et al.
Synthesis, 2003(13), 2001-2004 (2003)
One-pot synthesis of pyrrolo [1, 2-a] quinoxaline derivatives via iron-promoted aryl nitro reduction and aerobic oxidation of alcohols.
Pereira M D F and Thiery V
Organic Letters, 14(18), 4754-4757 (2012)
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