추천 제품
양식
powder
Quality Level
mp
228.65 °C
SMILES string
[Cs]F.Cl[C+]1=[N](C2=C(C(C)C)C=CC=C2C(C)C)C=CN1C3=C(C(C)C)C=CC=C3C(C)C.[Cl-]
InChI
1S/C27H36ClN2.ClH.Cs.FH/c1-17(2)21-11-9-12-22(18(3)4)25(21)29-15-16-30(27(29)28)26-23(19(5)6)13-10-14-24(26)20(7)8;;;/h9-20H,1-8H3;1H;;1H/q+1;;+1;/p-2
InChI key
AHNDOFVAHQKSBA-UHFFFAOYSA-L
일반 설명
PhenoFluor™ Mix is a mixture of N,N′-1,3-bis(2,6-diisopropylphenyl)chloroimidazolium chloride and CsF in 1:2 weight ratio.
애플리케이션
PhenoFluor™ Mix is a benchtop stable alternative to PhenoFluor™, which is a reagent for the deoxyfluorination of phenols, including electron-deficient, electron-rich, and heterocyclic phenols. Deoxyfluorination with PhenoFluor™ Mix is operationally simple and scalable.
기타 정보
Mix well, before use. Material can separate when not in use.
법적 정보
PhenoFluor is a trademark of SciFluor Life Sciences, LLC
PhenoFluor is a trademark of SciFluor Life Sciences, LLC
관련 제품
제품 번호
설명
가격
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3
표적 기관
Kidney,Adrenal gland, Respiratory system
보충제 위험성
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Facile C-F Bond Formation through a Concerted Nucleophilic Aromatic Substitution Mediated by the PhenoFluor Reagent.
Neumann CN and Ritter T
Accounts of Chemical Research, 50(11), 2822-2833 (2017)
PhenoFluorMix: practical chemoselective deoxyfluorination of phenols.
Fujimoto T and Ritter T
Organic Letters, 17(3), 544-547 (2015)
AlkylFluor: Deoxyfluorination of Alcohols.
Goldberg NW, et al.
Organic Letters, 18(23), 6102-6104 (2016)
관련 콘텐츠
An organic reaction toolbox provides structure-activity relationships for unique chemical reactions to optimally design and control small molecule synthesis.
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