19924-24-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound is in a liquid state and has no color.
Explanation
The compound has a mild and agreeable smell.
Explanation
The compound does not dissolve in water but can dissolve in organic solvents like alcohols, ethers, and hydrocarbons.
Explanation
The compound is used in various consumer products for its scent and flavor, as well as a solvent and a starting material for creating other compounds.
Explanation
Exposure to the compound through inhalation, ingestion, or skin contact may pose health risks, necessitating proper handling and safety precautions.
Explanation
When working with this chemical, it is essential to follow safety guidelines to minimize the risk of exposure and potential health hazards.
Physical state
Colorless liquid
Odor
Faint, pleasant
Solubility
Insoluble in water, soluble in organic solvents
Uses
Fragrance and flavor ingredient, solvent, intermediate in synthesis
Health hazards
Inhalation, ingestion, and skin contact
Safety precautions
Proper handling and safety measures required
Check Digit Verification of cas no
The CAS Registry Mumber 19924-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,2 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19924-24:
(7*1)+(6*9)+(5*9)+(4*2)+(3*4)+(2*2)+(1*4)=134
134 % 10 = 4
So 19924-24-4 is a valid CAS Registry Number.
19924-24-4Relevant articles and documents
REDOX REACTIONS OF 3,6-DI-TERT-BUTYL-ORTHO-BENZOQUINONE, CATALYZED BY TETRAFLUOROSILANE
Chekalov, A. K.,Gvazava, N. G.,Vol'eva, V. B.,Prokof'eva, T. I.,Prokof'ev, A. I.,Ershov, V. V.
, p. 991 - 993 (2007/10/02)
Tetrafluorosilane-catalyzed redox reactions of 3,6-di-tert-butyl-ortho-benzoquinone have been examined.From the EPR spectroscopic data and a study of the reaction products, a mechanism for these reactions is proposed involving the formation of a quinone-tetrafluorosilane complex which has strong oxidizing properties, and which enables the original quinone to undergo further reactions.
