7028-45-7 Usage
Chemical Structure
1,6-Hexanedione, 1,3,4,6-tetraphenyl-
Explanation
This structure indicates the arrangement of atoms in the molecule, with a six-carbon chain and two carbonyl groups (C=O) separated by the chain. The tetraphenyl groups are attached to the carbon atoms at positions 1, 3, 4, and 6.
Explanation
A diketone is an organic compound containing two carbonyl groups (C=O). In this case, the two carbonyl groups are separated by a six-carbon chain.
Explanation
1,6-Hexanedione, 1,3,4,6-tetraphenylis used as a starting material in the synthesis of other organic compounds, making it valuable for creating a variety of molecules in laboratory research.
Explanation
As a reagent, 1,6-Hexanedione, 1,3,4,6-tetraphenylis used to facilitate specific chemical reactions in organic chemistry, acting as a catalyst or reactant to produce desired products.
Explanation
This compound serves as a starting material for the preparation of pharmaceuticals and agrochemicals, which are chemicals used in the medical and agricultural industries, respectively.
Explanation
1,6-Hexanedione, 1,3,4,6-tetraphenylhas potential applications in material science as a precursor for the synthesis of polymers and other materials with specific properties and characteristics.
Explanation
The physical properties, such as melting point, boiling point, density, and solubility, are not provided in the given material.
Explanation
Information about the safety and handling precautions for 1,6-Hexanedione, 1,3,4,6-tetraphenylis not provided in the given material. It is essential to follow proper safety protocols when working with chemicals, especially in a laboratory setting.
Type of Compound
Diketone
Laboratory Research
Building block for synthesis
Reagent in Organic Chemistry
Facilitates reactions
Pharmaceutical and Agrochemical Applications
Starting material
Material Science Applications
Precursor for polymer synthesis
Physical Properties
Unknown (not provided in the material)
Safety and Handling
Unknown (not provided in the material)
Check Digit Verification of cas no
The CAS Registry Mumber 7028-45-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,2 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7028-45:
(6*7)+(5*0)+(4*2)+(3*8)+(2*4)+(1*5)=87
87 % 10 = 7
So 7028-45-7 is a valid CAS Registry Number.
7028-45-7Relevant articles and documents
Visible-Light-Driven Reductive (Cyclo)Dimerization of Chalcones over Heterogeneous Carbon Nitride Photocatalyst
Kurpil, Bogdan,Markushyna, Yevheniia,Savateev, Aleksandr
, p. 1531 - 1538 (2019/02/10)
Single-electron reduction of chalcones to the respective radical anions is a useful technique to activate these molecules toward subsequent transformations. Herein, a metal-free photocatalytic version of chalcones reduction in the presence of triethanolam
Aluminium chloride assisted zinc-induced reduction of some α,β-unsaturated ketones
Dey, Sankar P.
scheme or table, p. 761 - 763 (2010/08/19)
Some α,β-unsaturated ketones are reduced to give cyclodimerization products and/or β,β-coupling products in presence of Zn-AlCl3.6H2O-moist THF and aluminium chloride acts as Lewis acid to increase the yield of the products.
Synthesis of β-silylated olefins from α,β-unsaturated aldehydes and ketones
Bolourtchian,Mojtahedi,Saidi
, p. 590 - 591 (2007/10/03)
α,β-Unsaturated aldehydes and ketones such as phorone, benzalacetone, benzalacetophenone, 4-(2-furyl)-3-buten-4-one and β-ionone, react with TMS-Cl in the presence of Li in THF to give conjugated β-silylated enoxysilanes. Hydrolysis of this compounds in a
