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Documenti

903167

Sigma-Aldrich

10-Phenylphenothiazine

≥95%

Sinonimo/i:

10-Phenyl-10H-phenothiazine, N-Phenylphenothiazine

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About This Item

Formula empirica (notazione di Hill):
C18H13NS
Numero CAS:
7152-42-3
Peso molecolare:
275.37
Numero MDL:
MFCD00156238
Codice UNSPSC:
12352005

Saggio

≥95%

Forma fisica

powder

Impiego in reazioni chimiche

reagent type: catalyst
reaction type: Photocatalysis

Punto di fusione

94 °C

Attivazione fotocatalizzatore

365 nm

Stringa SMILE

C12=CC=CC=C1SC3=C(C=CC=C3)N2C4=CC=CC=C4

InChI

1S/C18H13NS/c1-2-8-14(9-3-1)19-15-10-4-6-12-17(15)20-18-13-7-5-11-16(18)19/h1-13H
WSEFYHOJDVVORU-UHFFFAOYSA-N

Categorie correlate

Applicazioni

An organic photo-catalyst used in synthesis of small molecules as well as polymerization reactions.

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

Altre note

Catalytic Defluoroalkylation of Trifluoromethylaromatics with Unactivated Alkenes

Single-Ion Homopolymer Electrolytes with High Transference Number Prepared by Click Chemistry and Photoinduced Metal-Free Atom-Transfer Radical Polymerization

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N° Catalogo
Descrizione
Determinazione del prezzo

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PhenN O-PC™ B0301, New Iridium, ≥97%

901111

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916722

Phenyl-(benzo)phenothiazine

922641

Pr-DMQA[BF4], ≥95%

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Fluorinated polymers are important materials that are widely used in many areas. Herein, we report the development of a metal-free photocontrolled radical polymerization of semifluorinated (meth)acrylates with a new visible-light-absorbing organocatalyst. This method enabled the production of a variety of
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We describe a new catalytic approach to selective functionalization of the strong C-F bonds in trifluoromethylaromatic (Ar-CF3) systems. In this approach, single electron reduction of Ar-CF3 substrates (using a photoredox catalyst) results in difluorobenzylic radical formation through a C-F cleavage
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