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Merck
모든 사진(2)

문서

909343

Sigma-Aldrich

2-(4-Fluorophenyl)-5-methylpyridine

≥95%

동의어(들):

p-F(Me)ppy

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모든 사진(2)

About This Item

실험식(Hill 표기법):
C12H10FN
CAS Number:
85237-65-6
Molecular Weight:
187.21
MDL number:
MFCD09037512
UNSPSC 코드:
12352101

분석

≥95%

형태

powder or crystals

반응 적합성

reaction type: Photocatalysis
reagent type: catalyst

mp

58-59 °C

InChI

1S/C12H10FN/c1-9-2-7-12(14-8-9)10-3-5-11(13)6-4-10/h2-8H,1H3

InChI key

WSVYYUKIXFSDTE-UHFFFAOYSA-N

애플리케이션

2-(4-Fluorophenyl)-5-methylpyridine is a ligand used for the preparation of Ir(III) photocatalysts.

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

기타 정보

Highly Fluorinated Ir(III)−2,2′:6′,2″−Terpyridine-Phenylpyridine−X Complexes via Selective C−F Activation: Robust Photocatalysts for Solar Fuel Generation and Photoredox Catalysis

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

Jonathan A Porras et al.
Journal of the American Chemical Society, 138(30), 9460-9472 (2016-07-09)
A series of fluorinated Ir(III)-terpyridine-phenylpyridine-X (X = anionic monodentate ligand) complexes were synthesized by selective C-F activation, whereby perfluorinated phenylpyridines were readily complexed. The combination of fluorinated phenylpyridine ligands with an electron-rich tri-tert-butyl terpyridine ligand generates a "push-pull" force on
Yufan Liang et al.
Nature, 559(7712), 83-88 (2018-06-22)
Over the past three decades, considerable progress has been made in the development of methods to construct sp2 carbon-nitrogen (C-N) bonds using palladium, copper or nickel catalysis1,2. However, the incorporation of alkyl substrates to form sp3 C-N bonds remains one
Andrew G Capacci et al.
Nature chemistry, 9(11), 1073-1077 (2017-10-25)
Although the α-alkylation of ketones has already been established, the analogous reaction using aldehyde substrates has proven surprisingly elusive. Despite the structural similarities between the two classes of compounds, the sensitivity and unique reactivity of the aldehyde functionality has typically
Yong Yao Loh et al.
Science (New York, N.Y.), 358(6367), 1182-1187 (2017-11-11)
Deuterium- and tritium-labeled pharmaceutical compounds are pivotal diagnostic tools in drug discovery research, providing vital information about the biological fate of drugs and drug metabolites. Herein we demonstrate that a photoredox-mediated hydrogen atom transfer protocol can efficiently and selectively install

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