Phenoxazine, 97%

Name: Phenoxazine, 97% | 135-67-1
Brand: J&K Chemical
SKU: JK398810_1_G
Price: 37.1 USD
Availability: OutOfStock

Cat. No JK398810_1_G

Vendor: J&K Chemical

Product Information

Product Name

Phenoxazine, 97%

Brand Name

J&K

Product Number

398810

CAS

135-67-1

Molecular Formula

C12H9NO

Molecular Weight

183.21

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

67278

IUPAC Name

10H-phenoxazine

InChI Key

TZMSYXZUNZXBOL-UHFFFAOYSA-N

SMILES

C1=CC=C2C(=C1)NC3=CC=CC=C3O2

Properties

Melting Point

156-159

Safety Information

Precautionary Statement

P262

References Data Source From Pubchem

Donor moiety engineering in D-D-π-A-π-A quinoxaline sensitizers for efficient dye-sensitized solar cells

Publication Name: Optical and Quantum Electronics

Publication Date: 2026-03-03

DOI: 10.1007/s11082-026-08731-5

Synthesis of 2-(3,5-diarylaminophenyl)-2h-benzo[d][1,2,3]triazoles With Aggregation Induced Emission Properties and Its Applications as a Blue OLED Component

Publication Name: Journal of Fluorescence

Publication Date: 2026-02-26

DOI: 10.1007/s10895-025-04703-2

Electrochemical properties of electrode coatings based on polyphenothiazine and polyphenoxazine and their composites with reduced graphene oxide in lithium organic electrolyte

Publication Name: Journal of Materials Research

Publication Date: 2026-02-04

DOI: 10.1557/s43578-026-01790-0

Versatile pyrazine derivatives with robust nonlinear optical (NLO) performance: symmetrical design and theoretical exploration

Publication Name: Structural Chemistry

Publication Date: 2026-01-21

DOI: 10.1007/s11224-026-02720-w

Exploring the NLO potential of new designed thieno[2,3-b]indole-based derivatives via donor group modification: a DFT study on static and frequency-dependent NLO properties

Publication Name: Journal of Computational Electronics

Publication Date: 2026-01-10

DOI: 10.1007/s10825-025-02486-0

Phenoxazine, 97%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Donor moiety engineering in D-D-π-A-π-A quinoxaline sensitizers for efficient dye-sensitized solar cells

Synthesis of 2-(3,5-diarylaminophenyl)-2h-benzo[d][1,2,3]triazoles With Aggregation Induced Emission Properties and Its Applications as a Blue OLED Component

Electrochemical properties of electrode coatings based on polyphenothiazine and polyphenoxazine and their composites with reduced graphene oxide in lithium organic electrolyte

Versatile pyrazine derivatives with robust nonlinear optical (NLO) performance: symmetrical design and theoretical exploration

Exploring the NLO potential of new designed thieno[2,3-b]indole-based derivatives via donor group modification: a DFT study on static and frequency-dependent NLO properties

Phenoxazine, 97%

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Phenoxazine, 97%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Donor moiety engineering in D-D-π-A-π-A quinoxaline sensitizers for efficient dye-sensitized solar cells

Synthesis of 2-(3,5-diarylaminophenyl)-2h-benzo[d][1,2,3]triazoles With Aggregation Induced Emission Properties and Its Applications as a Blue OLED Component

Electrochemical properties of electrode coatings based on polyphenothiazine and polyphenoxazine and their composites with reduced graphene oxide in lithium organic electrolyte

Versatile pyrazine derivatives with robust nonlinear optical (NLO) performance: symmetrical design and theoretical exploration

Exploring the NLO potential of new designed thieno[2,3-b]indole-based derivatives via donor group modification: a DFT study on static and frequency-dependent NLO properties

Phenoxazine, 97%

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