6338-86-9 Usage
Physical state
Yellow solid at room temperature
Common use
Intermediate in the synthesis of pharmaceuticals and other organic compounds
Structural features
Contains a sulfonyl group attached to a pentane-2,4-dione moiety
Chemical reactivity
Useful in a variety of chemical reactions due to its chemical structure
Safety precautions
Handle with caution and use proper safety measures, as it can be hazardous if not handled properly
Molecular weight
Approximately 270.31 g/mol (calculated from the chemical formula)
Solubility
Soluble in organic solvents like dichloromethane, ethyl acetate, and acetone
Melting point
Varies depending on the specific synthesis and purification method, but generally has a high melting point
Boiling point
High boiling point, typically above 300°C, due to its molecular structure and size
Density
Relatively high density, as it is a solid at room temperature and has a large molecular weight
Stability
Stable under normal conditions, but can decompose upon exposure to heat, light, or strong acids and bases
Environmental impact
May have an environmental impact if released into the environment, so proper disposal and containment measures should be taken
Storage
Store in a cool, dry, and well-ventilated area, away from heat, light, and incompatible substances
Check Digit Verification of cas no
The CAS Registry Mumber 6338-86-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6338-86:
(6*6)+(5*3)+(4*3)+(3*8)+(2*8)+(1*6)=109
109 % 10 = 9
So 6338-86-9 is a valid CAS Registry Number.
6338-86-9Relevant academic research and scientific papers
Ru-Catalyzed Chemo- and Enantioselective Hydrogenation of β-Diketones Assisted by the Neighboring Heteroatoms
Li, Wanfang,Lu, Bin,Xie, Xiaomin,Zhang, Zhaoguo
supporting information, p. 5509 - 5513 (2019/08/01)
A highly chemo- and enantioselective hydrogenation of β-diketones was achieved by using [Ru(benzene)(S)-SunPhosCl]Cl for consistency in THF. The neighboring heteroatoms played important roles in guaranteeing the reactivity and controlling the chemoselectivity. These results suggested a potential approach for the clean and facile synthesis of functionalized chiral β-hydroxy ketones, which could otherwise be prepared through much less step-economic transformations.
