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oxazine 1 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

47367-75-9

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47367-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 47367-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,3,6 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 47367-75:
(7*4)+(6*7)+(5*3)+(4*6)+(3*7)+(2*7)+(1*5)=149
149 % 10 = 9
So 47367-75-9 is a valid CAS Registry Number.
InChI:InChI=1/2C20H26N3O.4ClH.Zn/c2*1-5-22(6-2)15-9-11-17-19(13-15)24-20-14-16(23(7-3)8-4)10-12-18(20)21-17;;;;;/h2*9-14H,5-8H2,1-4H3;4*1H;/q2*+1;;;;;+2/p-4/r2C20H26N3O.Cl4Zn/c2*1-5-22(6-2)15-9-11-17-19(13-15)24-20-14-16(23(7-3)8-4)10-12-18(20)21-17;1-5(2,3)4/h2*9-14H,5-8H2,1-4H3;/q2*+1;-2

47367-75-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name oxazine-1

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:47367-75-9 SDS

47367-75-9Downstream Products

47367-75-9Relevant articles and documents

Phenoxazine-based Near-infrared Fluorescent Probes for the Specific Detection of Copper (II) Ions in Living Cells

Shen, Yang,Zheng, Wubin,Yao, Yusi,Wang, Dongmei,Lv, Guanglei,Li, Chunxia

, p. 2864 - 2867 (2020)

Abstract: It is well known that copper ions play a critical role in various physiological processes. However, a variety of human diseases are tightly correlated with copper overload. Although there are numerous fluorescent probes capable of detecting copper ions, most of them are “turn-off” probes owing to copper (II) ions fluorescence quenching effect, resulting in poor sensitivity. Herein, a novel “turn-on” near-infrared (NIR) fluorescent probe PZ-N based on phenoxazine was designed and synthesized for the selective detection of copper (II) ions (Cu2+). Upon the addition of Cu2+, the probe could quickly react with Cu2+ and emit strong fluorescence, along with colour change from colourless to obvious blue. Moreover, the probe PZ-N showed good water solubility, high selectivity, and excellent sensitivity with low limit of detection (1.93 nM) towards copper (II) ions. More importantly, PZ-N was capable of effectively detecting Cu2+ in living cells.

The near-infrared fluorescent probes based on phenoxazine for the rapid detection of hypochlorous acid

Hao, Shiyou,Li, Chunxia,Lv, Guanglei,Shen, Yang,Yang, Jiajia,Yao, Yusi,Zheng, Wubin

, (2020)

Hypochlorous acid (HOCl) is tightly related with a series of diseases, and plays an important part in biological processes. Herein, we designed and synthesized two “turn-on” near-infrared (NIR) probes (BC-2 and BC-3) based on phenoxazine to sense and imag

Synthesis and radiation sensitivity of phenoxazine type color formers including thiol ester protective group

Tachikawa, Tatsuya,Sato, Yohei,Tokita, Sumio

, p. 161/[461]-166/[466] (2007/10/03)

3,7-Bis(N,N-diethylamino)-10-(phenylthio)carbonylphenoxazine (1a) and its analogs (1b-f) were synthesized and the color change after γ irradiation was investigated. The color change of acetonitrile solutions of 1a ([1a] 0 = 1.0 × 10-3 M) after γ irradiation was identified by naked eyes at the dose of 20 Gy. Phenylthio-substituted compound la showed more significant absorbance increase than phenoxy-substituted compound, 3,7-bis(N,N-diethylamino)-10-phenoxycarbonylphenoxazine (2a). The C-S cleavage in la by γ irradiation was revealed to occur more easily than the C-O cleavage in 2a. The sensitivity of the color formers 1a-f) to γ rays was correlated with the stability of the thiyl radicals generated in the reaction.

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