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Merck

795291

Sigma-Aldrich

Phenofluor 溶液

0.1 M in toluene

别名:

1,3-Bis(2,6-diisopropylphenyl)-2,2-difluoro-4-imidazoline

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About This Item

经验公式(希尔记法):
C27H36F2N2
分子量:
426.58
MDL號碼:
分類程式碼代碼:
12352101
PubChem物質ID:
NACRES:
NA.22

形狀

liquid

品質等級

濃度

0.1 M in toluene

密度

0.865 g/mL at 25 °C

儲存溫度

2-8°C

InChI

1S/C27H36F2N2/c1-17(2)21-11-9-12-22(18(3)4)25(21)30-15-16-31(27(30,28)29)26-23(19(5)6)13-10-14-24(26)20(7)8/h9-20H,1-8H3

InChI 密鑰

FQXXWTOSPDVNSG-UHFFFAOYSA-N

應用

Facile deoxyfluorination of phenols without preactivation (), along with highly chemoselective deoxyfluorination of highly functionalized late-stage intermediates ().

法律資訊

PhenoFluor is a trademark of SciFluor Life Sciences, LLC
PhenoFluor is a trademark of SciFluor Life Sciences, LLC

相關產品

产品编号
说明
价格

訊號詞

Danger

危險分類

Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

標靶器官

Central nervous system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

39.2 °F

閃點(°C)

4 °C


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分析证书(COA)

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其他客户在看

Filippo Sladojevich et al.
Journal of the American Chemical Society, 135(7), 2470-2473 (2013-02-13)
An operationally simple protocol for the selective deoxyfluorination of structurally complex alcohols is presented. Several fluorinated derivatives of natural products and pharmaceuticals have been prepared to showcase the potential of the method for late-stage diversification and its functional group compatibility.
Pingping Tang et al.
Journal of the American Chemical Society, 133(30), 11482-11484 (2011-07-09)
An operationally simple ipso fluorination of phenols with a new deoxyfluorination reagent is presented.

商品

The functional-group-tolerant, one-step conversion of phenols to aryl fluorides is a highly desirable process. PhenoFluor™ solution, provides straightforward method to fluorinate alcohol and phenols without preactivation and regioselectively fluorinate highly functionalized late-stage intermediates.

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