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903167

Sigma-Aldrich

10-Phenylphenothiazine

≥95%

Sinonimo/i:

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

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100 MG
CHF 81.80
250 MG
CHF 165.00

CHF 81.80

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100 MG
CHF 81.80
250 MG
CHF 165.00

About This Item

Formula empirica (notazione di Hill):
C18H13NS
Numero CAS:
7152-42-3
Peso molecolare:
275.37
Numero MDL:
MFCD00156238
Codice UNSPSC:
12352005
NACRES:
NA.22

CHF 81.80

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Saggio

≥95%

Stato

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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Descrizione
Determinazione del prezzo

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901111

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916722

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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

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Certificati d'analisi (COA)

Lot/Batch Number
MKCR9957
MKCP3721
MKCH4612
MKCP0076

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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
Single-Ion Homopolymer Electrolytes with High Transference Number Prepared by Click Chemistry and Photoinduced Metal-Free Atom-Transfer Radical Polymerization.
Li. S, et al.
ACS Energy Letters, 3(1), 20-27 (2018)
Photocontrolled Growth of Cross-Linked Nanonetworks.
Lampley M W, et al.
ACS Macro Letters, 7(6), 745-750 (2018)
Mao Chen et al.
ACS central science, 3(2), 124-134 (2017-03-11)
Light-initiated additive manufacturing techniques typically rely on layer-by-layer addition or continuous extraction of polymers formed via nonliving, free radical polymerization methods that render the final materials "dead" toward further monomer insertion; the polymer chains within the materials cannot be reactivated
Hengbin Wang et al.
Journal of the American Chemical Society, 140(1), 163-166 (2017-12-20)
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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