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703540

Sigma-Aldrich

2,2,6,6-四甲基哌啶基氯化镁氯化锂复合物 溶液

1.0 M in THF/toluene

同義詞:

TMPMgCl·LiCl

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About This Item

經驗公式(希爾表示法):
C9H18Cl2LiMgN
CAS號碼:
分子量::
242.40
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

形狀

liquid

品質等級

反應適用性

reaction type: Grignard Reaction

濃度

1.0 M in THF/toluene
20 % (w/w)

密度

0.96 g/mL at 25 °C

儲存溫度

2-8°C

SMILES 字串

[Li+].[Cl-].CC1(C)CCCC(C)(C)N1[Mg]Cl

InChI

1S/C9H18N.2ClH.Li.Mg/c1-8(2)6-5-7-9(3,4)10-8;;;;/h5-7H2,1-4H3;2*1H;;/q-1;;;+1;+2/p-2

InChI 密鑰

JHBZAAACZVPPRQ-UHFFFAOYSA-L

應用

2,2,6,6-四甲基哌啶基氯化镁氯化锂复合物是非亲核性Knochel-Hauser碱, 主要用于官能化芳烃和杂芳烃的氧化,以制备相应的格氏试剂。它还可以用作通过催化剂转移缩聚合成Π-共轭聚合物过程的碱。

包裝

建议将25 mL Sure/Seal 瓶作为一次性包装瓶使用。 反复穿刺可能导致产品性能下降。

法律資訊

Albemarle US Inc.产品
Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

訊號詞

Danger

危險分類

Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Repr. 2 - Skin Corr. 1B

安全危害

儲存類別代碼

4.3 - Hazardous materials, which set free flammable gases upon contact with water

水污染物質分類(WGK)

WGK 3

閃點(°F)

5.0 °F

閃點(°C)

-15 °C


分析證明 (COA)

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Synthesis of fully substituted pyrazoles via regio-and chemoselective metalations.
Despotopoulou C
Organic Letters, 11(15), 3326-3329 (2009)
Conjugated Polymers with Repeated Sequences of Group 16 Heterocycles Synthesized through Catalyst-Transfer Polycondensation.
Tsai CH
Journal of the American Chemical Society, 138(21), 6798-6804 (2016)
Synthesis of polyfuran and thiophene-furan alternating copolymers using catalyst-transfer polycondensation.
Qiu Y
ACS Macro Letters, 5(3), 332-336 (2016)
Scaleable preparation of functionalized organometallics via directed ortho metalation using Mg-and Zn-amide bases.
Wunderlich SH
Organic Process Research & Development, 14(2), 339-345 (2010)
Hiroki Iguchi et al.
Scientific reports, 7, 39937-39937 (2017-01-07)
Processing and manipulation of highly conductive pristine graphene in large quantities are still major challenges in the practical application of graphene for electric device. In the present study, we report the liquid-phase exfoliation of graphite in toluene using well-defined poly(3-hexylthiophene)

文章

Transformative reagents for selective metalation, deprotonation and nucleophilic additions have allowed for unprecedented selective converstions to reactive intermediates within a molecule which contains sensative functionalities under mild reactions.

Transformative reagents for selective metalation, deprotonation and nucleophilic additions have allowed for unprecedented selective converstions to reactive intermediates within a molecule which contains sensative functionalities under mild reactions.

Sigma-Aldrich.com presents an article concerning New Reagents for Selective Metalation, Deprotonation, and 1,2-Additions.

Sigma-Aldrich.com presents an article concerning New Reagents for Selective Metalation, Deprotonation, and 1,2-Additions.

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