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Merck
모든 사진(1)

문서

P14858

Sigma-Aldrich

Phenoxazine

97%

동의어(들):

5,6-Dibenzo-1,4-oxazine

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C12H9NO
CAS Number:
135-67-1
Molecular Weight:
183.21
Beilstein:
143234
EC Number:
205-210-8
MDL number:
MFCD00005014
UNSPSC 코드:
12352100
PubChem Substance ID:
24898206
NACRES:
NA.22

분석

97%

형태

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

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

시험 성적서(COA)

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문서 라이브러리 방문

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.
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
Seelam Venkata Reddy et al.
Bioorganic & medicinal chemistry, 21(7), 1952-1963 (2013-02-19)
A number of novel imidazophenoxazine-4-sulfonamides have been designed as potential inhibitors of PDE4. All these compounds were readily prepared via an elegant multi-step method involving the initial construction of 1-nitro-10H-phenoxazine ring and then fused imidazole ring as key steps. Some
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.
Riyad Ahmed Al-Okab et al.
Journal of hazardous materials, 170(1), 292-297 (2009-05-30)
Novel, sensitive and rapid spectrophotometric methods, using phenoxazine (PNZ), 2-chlorophe-noxazine (CPN) and 2-trifluoromethylphenoxazine (TPN) as chromogenic reagents for the determination of residual chlorine are proposed. The methods are based on the reduction of chlorine by an electrophilic coupling reagent, 3-methyl-2-benzothiazoline
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