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Merck
CN

P14831

Phenothiazine

≥98%

Synonym(s):

Dibenzo-1,4-thiazine, Thiodiphenylamine, 10H-Phenothiazine

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About This Item

Empirical Formula (Hill Notation):
C12H9NS
CAS Number:
92-84-2
Molecular Weight:
199.27
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
24898205
EC Number:
202-196-5
Beilstein/REAXYS Number:
143237
MDL number:
MFCD00005015
Assay:
≥98%
Bp:
371 °C (lit.)

Key Documents

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Product Name

Phenothiazine, ≥98%

InChI key

WJFKNYWRSNBZNX-UHFFFAOYSA-N

InChI

1S/C12H9NS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H

SMILES string

N1c2ccccc2Sc3ccccc13

assay

≥98%

bp

371 °C (lit.)

mp

182-187 °C (lit.)

Quality Level

200

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Application

Phenothiazine can be used in the following applications:
  • It can be connected to carbazole by C-N linkage to increase the hole mobility and thermal stability in organic light-emitting devices.
  • Used in the fabrication of CMA-based (Carbene-Metal-Amide) white light-emitting OLED.
  • It is used as a starting material in the synthesis of dialdehyde monomer. A conjugated copolymer is prepared using this dialdehyde monomer, which is applicable as an emitting layer in PLED.
  • Used as a building block in the synthesis of conjugated dendrimers, for the development of light-emitting devices.

General description

Phenothiazine is a versatile building block that can be easily functionalized as it possesses multiple modification sites. Its unique butterfly configuration and electron-rich character are beneficial for its potential use in optoelectronic applications. As it can undergo fast and reversible electron transfer reactions, it is widely used as photoactive material in organic light-emitting devices and solar cells.

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2 Oral

target_organs

Blood

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ5642
MKCZ2613
MKCZ3361
MKCZ2474
MKCZ1848

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Indian J. Chem. B, 33, 397-397 (1994)
Alexander S Romanov et al.
Chemical science, 11(2), 435-446 (2020-03-20)
Conformationally flexible "Carbene-Metal-Amide" (CMA) complexes of copper and gold have been developed based on a combination of sterically hindered cyclic (alkyl)(amino)carbene (CAAC) and 6- and 7-ring heterocyclic amide ligands. These complexes show photoemissions across the visible spectrum with PL quantum
Mol. Cryst. Liq. Cryst. Sci. Technol., Sect. A, 237, 419-419 (1993)
Synthesis of p-type conjugated dendrimers bearing phenothiazine moiety at the periphery and their light-emitting device characterization
Dong Hoon Choi, et al.
Synthetic Metals, 157(8), 332-335 (2007)
Structure-induced optoelectronic properties of phenothiazine-based materials
Revoju, et al.
Journal of Material Chemistry C, 8(44), 15486-15506 (2020)
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