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903167

Sigma-Aldrich

10-Phenylphenothiazine

≥95%

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C18H13NS
Número CAS:
7152-42-3
Peso molecular:
275.37
Número MDL:
MFCD00156238
Código UNSPSC:
12352005
NACRES:
NA.22

Ensaio

≥95%

forma

powder

adequação da reação

reagent type: catalyst
reaction type: Photocatalysis

pf

94 °C

ativação do fotocatalisador

365 nm

cadeia de caracteres SMILES

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

chave InChI

WSEFYHOJDVVORU-UHFFFAOYSA-N

Categorias relacionadas

Aplicação

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)

Outras notas

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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Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Honghong Gong et al.
Angewandte Chemie (International ed. in English), 57(1), 333-337 (2017-11-15)
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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