推荐产品
品質等級
濃度
2.0 M in toluene
密度
0.931 g/mL at 25 °C
SMILES 字串
C[Zn]C
InChI
1S/2CH3.Zn/h2*1H3;
InChI 密鑰
AXAZMDOAUQTMOW-UHFFFAOYSA-N
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應用
Dimethylzinc can be used as:
- A catalyst with nickel for the stereoselective C−2 alkenylation and dialkenylation of pyridine derivatives by alkynes to give monoalkenylation products.
- A reagent with aldehydes and 2-methoxyaniline for the enantioselective synthesis of alkyl and aralkyl secondary amines via one-pot three-component coupling reaction in the presence of zirconium tetraisopropoxide.
- A methylating reagent for the methylation of fluoroalkylated pyruvates in the presence of a copper/chiral diphosphine catalyst.
- An activator for radical trifluoromethylation of silyl enol ethers leading to α-trifluoromethyl ketones.
訊號詞
Danger
危險分類
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 - STOT SE 3 - Water-react 1
標靶器官
Central nervous system
儲存類別代碼
4.2 - Pyrophoric and self-heating hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
1.4 °F - closed cup
閃點(°C)
-17 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Organic letters, 8(21), 4671-4673 (2006-10-06)
[reaction: see text] The radical trifluoromethylation of ketone silyl enol ethers gave alpha-CF(3) ketones in good yields with wide scope of the ketonic substrates including acyclic ketones and cyclopentanone. The use of dialkylzinc to activate the silyl enol ethers is
Radical trifluoromethylation of ketone silyl enol ethers by activation with dialkylzinc.
Organic Letters, 8(21), 4671-4673 (2006)
A strategy for C-H activation of pyridines: direct C-2 selective alkenylation of pyridines by Nickel/Lewis Acid catalysis.
Journal of the American Chemical Society, 130(8), 2448-2449 (2008)
Three-component catalytic asymmetric synthesis of aliphatic amines.
Journal of the American Chemical Society, 123(42), 10409-10410 (2001)
Copper-catalyzed asymmetric methylation of fluoroalkylated pyruvates with dimethylzinc.
Beilstein Journal of Organic Chemistry, 14(1), 576-582 (2018)
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