69725-37-7 Usage
Uses
Used in Fragrance Industry:
2,2,7-TRIMETHYL-3,5-OCTANEDIONE is used as a fragrance ingredient for its distinctive scent profile, enhancing the aroma of various skincare and cosmetic products. Its ability to impart a pleasant and long-lasting fragrance makes it a valuable addition to the formulation of perfumes, lotions, and other personal care items.
Used in Sunscreen Products:
In the sunscreen industry, 2,2,7-TRIMETHYL-3,5-OCTANEDIONE is used as a UV-absorbing agent. Its capacity to absorb ultraviolet radiation effectively protects the skin from harmful UVA and UVB rays, reducing the risk of sunburn, premature aging, and skin cancer. This property makes it a crucial component in the development of sunscreens and other sun protection products.
Used in Organic Synthesis:
2,2,7-TRIMETHYL-3,5-OCTANEDIONE is utilized as a key intermediate in the synthesis of various organic compounds. Its reactivity and compatibility with other chemical entities allow for the creation of a wide range of molecules with diverse applications in pharmaceuticals, agrochemicals, and other specialty chemicals.
Used as a Reagent in Chemical Reactions:
In the field of chemistry, 2,2,7-TRIMETHYL-3,5-OCTANEDIONE serves as a reagent in various chemical reactions. Its ability to participate in condensation, oxidation, and reduction reactions makes it a valuable tool for chemists in the synthesis of complex organic molecules and the development of new chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 69725-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,2 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69725-37:
(7*6)+(6*9)+(5*7)+(4*2)+(3*5)+(2*3)+(1*7)=167
167 % 10 = 7
So 69725-37-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O2/c1-8(2)6-9(12)7-10(13)11(3,4)5/h8H,6-7H2,1-5H3
69725-37-7Relevant academic research and scientific papers
Nandurkar, Nitin S.,Bhanushali, Mayur J.,Patil, Dinkar S.,Bhanage, Bhalchandra M.
, p. 4111 - 4115 (2007)
An efficient and practical method for the synthesis of sterically hindered aliphatic/aromatic 1,3-diketones via coupling of ketones with esters using potassium tert-butoxide is described. The protocol requires milder operating conditions, and the products are obained in good to excellent yields. Copyright Taylor & Francis Group, LLC.
