102305-07-7 Usage
Chemical structure
1,2,3-Benzenetriol derivative with a methanesulfonate group attached
Explanation
The compound is derived from benzenetriol, which is a type of phenolic compound. The 1-methanesulfonate group is attached to the benzenetriol molecule, making it a methanesulfonate salt.
Explanation
It is an organic compound because it contains carbon and hydrogen atoms, along with other elements like oxygen and sulfur.
Explanation
The compound has three hydroxyl (OH) groups attached to the benzene ring, making it a phenolic compound. Additionally, it has a methanesulfonate group (-SO3CH3) attached to the benzene ring.
Explanation
This chemical is used as a reagent in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and other fine chemicals.
Explanation
Due to its chemical properties, 1,2,3-Benzenetriol, 1-methanesulfonate (9CI) can pose risks to human health and the environment if not handled with care and proper safety measures.
Explanation
The compound is soluble in water due to the presence of polar hydroxyl and methanesulfonate groups. It is also soluble in organic solvents like ethanol, methanol, and acetone.
Explanation
The compound is generally stable at room temperature and does not readily decompose or react with other substances under normal conditions.
Explanation
To maintain the stability and safety of the compound, it should be stored in a cool, dry, and well-ventilated area, away from heat, moisture, and direct sunlight.
Explanation
When handling 1,2,3-Benzenetriol, 1-methanesulfonate (9CI), it is essential to wear appropriate PPE, such as gloves, goggles, and a lab coat, and follow proper handling procedures to minimize the risk of exposure and potential hazards.
Type of compound
Organic compound
Functional groups
Phenolic hydroxyl groups, methanesulfonate group
Application
Reagent in organic synthesis
Hazardous nature
Potentially hazardous if not properly managed
Solubility
Soluble in water and organic solvents
Stability
Stable under normal conditions
Storage
Store in a cool, dry, and well-ventilated area
Safety precautions
Use personal protective equipment (PPE) and follow proper handling procedures
Check Digit Verification of cas no
The CAS Registry Mumber 102305-07-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,0 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102305-07:
(8*1)+(7*0)+(6*2)+(5*3)+(4*0)+(3*5)+(2*0)+(1*7)=57
57 % 10 = 7
So 102305-07-7 is a valid CAS Registry Number.
102305-07-7Relevant academic research and scientific papers
94. Synthesen von Dibenzodioxin-2,3-chinonen, einschliesslich der Ecklonochinone A und B sowie der Isoecklonochinone A und B
Luetolf, Walter Leo,Prewo, Roland,Bieri, Jost H.,Ruedi, Peter,Eugester, Conrad Hans
, p. 860 - 881 (2007/10/02)
Syntheses of Dibenzodioxin-2,3-quinones Including the Ecklonoquinones A and B and the Isoecklonoquinones A and B.Oxidation of monomesyloxy-substituted pyrocatechols with MnO2 in toluene using phase-transfer conditions leads in high yield to monomesyloxy-substituted dibenzodioxin-2,3-quinones with loss of one mesyloxy group.In this way, ecklonoquinone A (2), ecklonoquinone B (3), isoecklonoquinone A (43), and isoecklonoquinone B (44) were prepared.Their structures are based on X-ray analyses of ecklonoquinone-A leucoacetate (45) and the mesyloxy-substituted quinone 20.The reddish-violet dibenzodioxin-diquinone 49 was prepared from an intermediate of the iso-series.The parent compound 1 has been synthesized in yields better than 50percent from pyrocatechol and methyl 2,5-dioxo-2,5-dihydrobenzoate as oxidant and 2-methoxypyridin as catalyst.To rationalize the specific effect on the dimerisation step of the mesyloxy group, the intermediacy of 1,4-quinone monoacetals is proposed.This also applies to a proposed biogenetic scheme.
