5411-99-4 Usage
Uses
Used in Organic Synthesis:
2,6-dibromo-1,7-diphenylheptane-1,7-dione is used as a key intermediate in the synthesis of complex organic molecules. Its presence of bromine atoms and phenyl groups allows for a wide range of reactions, making it a versatile building block for the creation of new compounds.
Used in Chemical Reactions:
As a reagent, 2,6-dibromo-1,7-diphenylheptane-1,7-dione is employed in various chemical reactions to facilitate the formation of desired products. Its reactivity with other compounds can lead to the development of new materials and substances with specific properties.
Used in Pharmaceutical Applications:
2,6-dibromo-1,7-diphenylheptane-1,7-dione is used as a starting material or a component in the development of pharmaceuticals. Its unique structure and reactivity can contribute to the creation of new drugs with potential therapeutic applications.
Used in Agrochemical Applications:
In the agrochemical industry, 2,6-dibromo-1,7-diphenylheptane-1,7-dione is used as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its properties can be harnessed to develop more effective and environmentally friendly products.
Used in Materials Science:
2,6-dibromo-1,7-diphenylheptane-1,7-dione is used as a component in the development of new materials with specific properties, such as polymers, coatings, and adhesives. Its inclusion in these materials can enhance their performance and applicability in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5411-99-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5411-99:
(6*5)+(5*4)+(4*1)+(3*1)+(2*9)+(1*9)=84
84 % 10 = 4
So 5411-99-4 is a valid CAS Registry Number.
5411-99-4Relevant academic research and scientific papers
Reactions of Carbonyl Compounds with Benzyl Chloromethyl Ether of Diiodomethane in the Presence of Samarium(II) Iodide or Metallic Samarium. New Routes to 1,2-Diols, Iodohydrins and Cyclopropanols
Imamoto, Tsuneo,Hatajima, Toshihiko,Takiyama, Nobuyuki,Takeyama, Toshiaki,Kamiya, Yasuo,Yoshizawa, Takeshi
, p. 3127 - 3135 (2007/10/02)
Carbonyl compounds react with benzyl chloromethyl ether in the presence of samarium(II) iodide to afford the corresponding addition products which, when subsequently hydrogenolysed, yield 1,2-diols.Simple aldehydes and ketones react with diiodomethane in the presence of samarium metal to give iodohydrins in good yields.Under similar reaction conditions, α-halogeno substituted ketones and aromatic 1,4-diketones are converted into cyclopropanols.These cyclopropanations have been shown to rpoceed through the initial generation of samarium enolates, followed by the Simmons-Smith type reaction.A novel transformation of esters to cyclopropanols via tandem one-carbon homologation is also described.
