CAS 135-67-1|Phenoxazine

Introduction：Basic information about CAS 135-67-1|Phenoxazine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Phenoxazine BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Customs
6. Synonyms

Common Name	Phenoxazine
CAS Number	135-67-1	Molecular Weight	183.21
Density	1.2±0.1 g/cm3	Boiling Point	318.0±12.0 °C at 760 mmHg
Molecular Formula	C₁₂H₉NO	Melting Point	156-159 °C(lit.)
MSDS	/	Flash Point	122.6±9.0 °C

Names

Name	Phenoxazine
Synonym	More Synonyms

Phenoxazine BiologicalActivity

Description	Phenoxazine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog	Research Areas >>OthersSignaling Pathways >>Others >>Others
References	[1]. Shruti , Dwivedi, J., Kishore, D., et al.Recent advancement in the synthesis of phenoxazine derivatives and their analoguesSynthetic Commun.48(12)1377-1402(2018) [2]. Shimizu, S., Suzuki, M., Tomoda , A., et al.Phenoxazine compounds produced by the reactions with bovine hemoglobin show antimicrobial activity against non-tuberculosis mycobacteria Tohoku J. Exp. Med.203(1)47-52(2004) [3]. Che, X.-F., Zheng, C.-L., Akiyama, S.-I., et al. 2-Aminophenoxazine-3-one and 2-amino-4,4α-dihydro-4α,7-dimethyl-3H-phenoxazine-3-one cause cellular apoptosis by reducing higher intracellular pH in cancer cellsProc. Jpn. Acad. [4]. Ser, et al.Synthesis, structure and diverse coordination chemistry of cobalt(III) complexes derived from a Schiff base ligand and their biomimetic catalytic oxidation of o-aminophenolsPolyhedron16423-34(2019)

Description

Phenoxazine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Related Catalog

Research Areas >>OthersSignaling Pathways >>Others >>Others

References

[1]. Shruti , Dwivedi, J., Kishore, D., et al.Recent advancement in the synthesis of phenoxazine derivatives and their analoguesSynthetic Commun.48(12)1377-1402(2018)

[2]. Shimizu, S., Suzuki, M., Tomoda , A., et al.Phenoxazine compounds produced by the reactions with bovine hemoglobin show antimicrobial activity against non-tuberculosis mycobacteria Tohoku J. Exp. Med.203(1)47-52(2004)

[3]. Che, X.-F., Zheng, C.-L., Akiyama, S.-I., et al. 2-Aminophenoxazine-3-one and 2-amino-4,4α-dihydro-4α,7-dimethyl-3H-phenoxazine-3-one cause cellular apoptosis by reducing higher intracellular pH in cancer cellsProc. Jpn. Acad.

[4]. Ser, et al.Synthesis, structure and diverse coordination chemistry of cobalt(III) complexes derived from a Schiff base ligand and their biomimetic catalytic oxidation of o-aminophenolsPolyhedron16423-34(2019)

Chemical & Physical Properties

Density	1.2±0.1 g/cm3
Boiling Point	318.0±12.0 °C at 760 mmHg
Melting Point	156-159 °C(lit.)
Molecular Formula	C₁₂H₉NO
Molecular Weight	183.21
Flash Point	122.6±9.0 °C
Exact Mass	183.068420
PSA	21.26000
LogP	3.84
Vapour Pressure	0.0±0.7 mmHg at 25°C
Index of Refraction	1.625
InChIKey	TZMSYXZUNZXBOL-UHFFFAOYSA-N
SMILES	c1ccc2c(c1)Nc1ccccc1O2

Safety Information

Safety Phrases	S22-S24/25
WGK Germany	3
HS Code	2934999090

Customs

HS Code	2934999090
Summary	2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Synonyms

Phenoxazine

10H-Phenoxazine

10H-Phenoxazine (9CI)

EINECS 205-210-8

MFCD00005014

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