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P14858

Phenoxazine

Name: Phenoxazine
Brand: ALDRICH

97%

Synonym(s):

5,6-Dibenzo-1,4-oxazine

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About This Item

Empirical Formula (Hill Notation):

C₁₂H₉NO

CAS Number:

135-67-1

Molecular Weight:

183.21

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24898206

EC Number:

205-210-8

Beilstein/REAXYS Number:

143234

MDL number:

MFCD00005014

Assay:

97%

Form:

powder

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Properties

Quality Level

100

assay

97%

form

powder

mp

156-159 °C (lit.)

SMILES string

N1c2ccccc2Oc3ccccc13

InChI

1S/C12H9NO/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H

InChI key

TZMSYXZUNZXBOL-UHFFFAOYSA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Pro-oxidant effects of phenothiazine and phenoxazine on erythrocytes in the presence of peroxyl radical.

Guo-Xiang Li et al.

Journal of biochemical and molecular toxicology, 23(4), 280-286 (2009-08-26)

Phenothiazine (PtzNH) and phenoxazine (PozNH) can protect human erythrocytes against hemolysis induced by 2,2'-azobis(2-amidinopropane hydrochloride) (AAPH), a peroxyl radical supplier. However, an antioxidant may be a pro-oxidant to accelerate the oxidation in the presence of radicals. The aim of this

Palladium-catalyzed domino C-C/C-N coupling using a norbornene template: synthesis of substituted benzomorpholines, phenoxazines, and dihydrodibenzoxazepines.

Praew Thansandote et al.

The Journal of organic chemistry, 75(10), 3495-3498 (2010-04-29)

A rapid, four-step approach to alkyl- and aryl-substituted benzomorpholines is accomplished by a Pd-catalyzed domino C-C/C-N bond coupling using a norbornene template. Extension to phenoxazines and dihydrodibenzoxazepines is presented.

Molecular recognition of cationic phenothiazinium and phenoxazinium dyes with pi-extended 2'-deoxyadenosine nucleotides.

Karina Mondragón-Vásquez et al.

Chemical communications (Cambridge, England), (44)(44), 6726-6728 (2009-11-04)

N(6)-(N'-Arylcarbamoyl)-2'-deoxyadenosine-H-phosphonates displayed molecular recognition towards cationic phenothiazinium and phenoxazinium dyes in aqueous solutions; studies have shown that binding is driven mainly by aromatic interactions and that size and shape-complementarity of the aromatic rings in host and guest provides selectivity.

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Global Trade Item Number

SKU	GTIN
P14858-5G	04061833468852
P14858-1G	04061826677506