903167
10-Phenylphenothiazine
≥95%, powder
Synonym(s):
10-Phenyl-10H-phenothiazine, N-Phenylphenothiazine
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About This Item
Empirical Formula (Hill Notation):
C18H13NS
CAS Number:
Molecular Weight:
275.37
NACRES:
NA.22
UNSPSC Code:
12352005
MDL number:
Product Name
10-Phenylphenothiazine, ≥95%
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
SMILES string
C12=CC=CC=C1SC3=C(C=CC=C3)N2C4=CC=CC=C4
InChI key
WSEFYHOJDVVORU-UHFFFAOYSA-N
assay
≥95%
form
powder
reaction suitability
reagent type: catalyst
reaction type: Photocatalysis
mp
94 °C
photocatalyst activation
365 nm
Related Categories
Application
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)
Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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ACS Macro Letters, 7(6), 745-750 (2018)
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)
Honghong Gong et al.
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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
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
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