7622-31-3 Usage
Explanation
This is an alternative name for 1,3-Benzodioxol-5-ol, 6-methyl-, which is derived from its chemical structure.
Explanation
1,3-Benzodioxol-5-ol, 6-methylcan be found in these natural sources, which means it can be extracted from these plants for use in various applications.
Explanation
The compound has a pleasant scent that can be described as a combination of sweet and spicy notes.
Explanation
Due to its appealing aroma, 1,3-Benzodioxol-5-ol, 6-methylis used in the production of various consumer products, such as perfumes, soaps, and flavorings.
Explanation
Research is being conducted to determine the potential carcinogenic (cancer-causing) and toxic effects of 1,3-Benzodioxol-5-ol, 6-methylon humans and the environment.
Explanation
The compound's impact on the central nervous system is currently being studied to understand its potential effects on human health.
Explanation
Despite potential risks, 1,3-Benzodioxol-5-ol, 6-methylis still utilized in different industries. However, the use of 1,3-Benzodioxol-5-ol, 6-methyl- may be subject to regulations and restrictions based on the intended application and the specific industry.
Natural sources
Nutmeg, basil, and bay leaves
Aroma
Sweet, spicy
Applications
Perfumes, soaps, and flavorings
Potential risks
Carcinogenic and toxic properties
Effects on the central nervous system
Under investigation
Industry use
Various industries, with regulations and restrictions
Check Digit Verification of cas no
The CAS Registry Mumber 7622-31-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,2 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7622-31:
(6*7)+(5*6)+(4*2)+(3*2)+(2*3)+(1*1)=93
93 % 10 = 3
So 7622-31-3 is a valid CAS Registry Number.
7622-31-3Relevant academic research and scientific papers
Synthesis and Antioxidant Capacity of Some Derivatives of Sesamol at the C-6 Position
Buravlev, Evgeny V.,Shevchenko, Oksana G.,Suponitsky, Kyrill Yu.
, (2021/05/27)
Several synthetic approaches (aminomethylation, alkylation, condensation, etc.) have been used to synthesize derivatives based on the sesamol (1), natural phenol. The set of methods, including the study of antioxidant activity (AOA) by the ability to inhibit the initiated oxidation of animal lipids, radical scavenging activity, Fe2+-chelation ability, as well as a comparative assessment of membrane-protective activity under the conditions of H2O2-induced hemolysis of mice red blood cells (RBCs), was used to analyze the antioxidant potential of the synthesized compounds. The synthesized derivatives have demonstrated different activity in the listed test systems, and we have identified compounds which appear to be most promising for a detailed study of their pharmacological properties.
