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Acetic acid phenazin-1-yl ester, also known as phenazine acetate, is a chemical compound with the molecular formula C16H13N3O2. It is derived from phenazine, a heterocyclic compound with a tricyclic structure consisting of two benzene rings fused to a diazine ring. This ester is formed by the reaction of phenazine with acetic acid, resulting in the attachment of an acetate group to the nitrogen atom of the phenazine molecule. Phenazine acetate is a yellow crystalline solid that is soluble in organic solvents such as ethanol and chloroform. It has been used in various applications, including as a reagent in chemical synthesis and as a potential antimicrobial agent. However, it is important to note that the safety and efficacy of Acetic acid phenazin-1-yl ester in various applications should be evaluated through proper scientific research and testing.

6033-10-9

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6033-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6033-10-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,3 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6033-10:
(6*6)+(5*0)+(4*3)+(3*3)+(2*1)+(1*0)=59
59 % 10 = 9
So 6033-10-9 is a valid CAS Registry Number.

6033-10-9SDS

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 phenazin-1-yl acetate

1.2 Other means of identification

Product number -
Other names 1-Phenazinol,acetate (ester)

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:6033-10-9 SDS

6033-10-9Relevant academic research and scientific papers

Aerobic Dehydrogenation of N-Heterocycles with Grubbs Catalyst: Its Application to Assisted-Tandem Catalysis to Construct N-Containing Fused Heteroarenes

Kawauchi, Daichi,Noda, Kenta,Komatsu, Yoshiyuki,Yoshida, Kei,Ueda, Hirofumi,Tokuyama, Hidetoshi

supporting information, p. 15793 - 15798 (2020/10/12)

An aerobic dehydrogenation of nitrogen-containing heterocycles catalyzed by Grubbs catalyst is developed. The reaction is applicable to various nitrogen-containing heterocycles. The exceptionally high functional group compatibility of this method was confirmed by the oxidation of an unprotected dihydroindolactam V to indolactam V. Furthermore, by taking advantage of the oxygen-mediated structural change of the Grubbs catalyst, we integrated ring-closing metathesis and subsequent aerobic dehydrogenation to develop the novel assisted-tandem catalysis using molecular oxygen as a chemical trigger. The utility of the assisted-tandem catalysis was demonstrated by the concise synthesis of N-containing fused heteroarenes including a natural antibiotic, pyocyanine.

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