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1,6-Phenazinediol, 5-oxide, also known as 5-hydroxyphenazine-6-ol, is a chemical compound with the molecular formula C12H8N2O2. It is a derivative of phenazine, a heterocyclic compound consisting of a fused pyrazine and pyridazine ring system. This particular compound features a hydroxyl group at the 5-position and a hydroxyl group at the 6-position, with an additional oxygen atom at the 5-oxide position. 1,6-Phenazinediol, 5-oxide, is known for its various biological activities, such as antimicrobial and antitumor properties, and is found in certain bacteria and fungi. Its chemical structure and properties make it a subject of interest in the fields of organic chemistry, medicinal chemistry, and microbiology.

69-86-3

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69-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69-86-3 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69-86:
(4*6)+(3*9)+(2*8)+(1*6)=73
73 % 10 = 3
So 69-86-3 is a valid CAS Registry Number.

69-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dihydroxyphenazin-1-one

1.2 Other means of identification

Product number -
Other names 1,6-Phenazinediol,5-oxide

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:69-86-3 SDS

69-86-3Relevant academic research and scientific papers

Dual phenazine gene clusters enable diversification during biosynthesis

Shi, Yi-Ming,Brachmann, Alexander O.,Westphalen, Margaretha A.,Neubacher, Nick,Tobias, Nicholas J.,Bode, Helge B.

, p. 331 - 339 (2019/04/17)

Biosynthetic gene clusters (BGCs) bridging genotype and phenotype continuously evolve through gene mutations and recombinations to generate chemical diversity. Phenazine BGCs are widespread in bacteria, and the biosynthetic mechanisms of the formation of the phenazine structural core have been illuminated in the last decade. However, little is known about the complex phenazine core-modification machinery. Here, we report the diversity-oriented modifications of the phenazine core through two distinct BGCs in the entomopathogenic bacterium Xenorhabdus szentirmaii, which lives in symbiosis with nematodes. A previously unidentified aldehyde intermediate, which can be modified by multiple enzymatic and non-enzymatic reactions, is a common intermediate bridging the pathways encoded by these BGCs. Evaluation of the antibiotic activity of the resulting phenazine derivatives suggests a highly effective strategy to convert Gram-positive specific phenazines into broad-spectrum antibiotics, which might help the bacteria–nematode complex to maintain its special environmental niche.

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