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Merck
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文件

900941

Sigma-Aldrich

氯(4-氰基苯基)[(R)-1-[(S)-2-[双(4-氟苯基]膦基]二茂铁基]乙基二--丁基膦]镍(II)

≥95%

同義詞:

SK-J014-1n

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About This Item

經驗公式(希爾表示法):
C39H42ClF2FeNNiP2
CAS號碼:
分子量::
774.69
分類程式碼代碼:
12352103
NACRES:
NA.22

品質等級

化驗

≥95%

形狀

powder or solid

反應適用性

core: nickel
reaction type: Cross Couplings
reagent type: catalyst

SMILES 字串

CC(C)(C)P(C(C)(C)C)C[C]1[C][C][C][C]1P(C2=CC=C(F)C=C2)C3=CC=C(F)C=C3.Cl[Ni]C4=CC=C(C#N)C=C4.[C]5[C][C][C][C]5.[Fe]

相關類別

應用

Amination of functionalized aryl chlorides with ammonia and ammonium salts.

訊號詞

Warning

危險聲明

危險分類

Aquatic Chronic 2 - Repr. 2 - Skin Irrit. 2

儲存類別代碼

4.1B - Flammable solid hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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存取文件庫

Ni?Catalyzed Amination Reactions: An Overview.
Marin M, et al.
Chemical Record, 16(4), 1819-1832 (2016)
Evaluating 1, 1?-Bis (phosphino) ferrocene Ancillary Ligand Variants in the Nickel-Catalyzed C?N Cross-Coupling of (Hetero) aryl Chlorides.
Clark J S, et al.
Organometallics, 36(3), 679-686 (2017)
Nickel?Catalyzed Monoarylation of Ammonia.
Borzenko A, et al.
Angewandte Chemie (International Edition in English), 54(12), 3773-3777 (2015)
Nickel?Catalyzed Amination of Aryl Chlorides with Ammonia or Ammonium Salts.
Green R A and Hartwig J F
Angewandte Chemie (International Edition in English), 54(12), 3768-3772 (2015)
Sarah Z Tasker et al.
Nature, 509(7500), 299-309 (2014-05-16)
Tremendous advances have been made in nickel catalysis over the past decade. Several key properties of nickel, such as facile oxidative addition and ready access to multiple oxidation states, have allowed the development of a broad range of innovative reactions.

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