69404-97-3 Usage
Uses
Used in Pharmaceutical Industry:
2-(TERT-BUTYLDIMETHYLSILOXY)PENT-2-EN-4-ONE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its reactivity and stability enable the production of complex molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(TERT-BUTYLDIMETHYLSILOXY)PENT-2-EN-4-ONE is utilized as a precursor for the development of novel agrochemicals. Its unique properties allow for the creation of innovative compounds with improved efficacy and selectivity in crop protection.
Used in Materials Science:
2-(TERT-BUTYLDIMETHYLSILOXY)PENT-2-EN-4-ONE is employed as a building block in the synthesis of advanced materials with specific properties. Its versatility in organic synthesis contributes to the development of materials with applications in various fields, such as electronics, coatings, and adhesives.
Used as a Cross-Coupling Reagent:
In chemical research and development, 2-(TERT-BUTYLDIMETHYLSILOXY)PENT-2-EN-4-ONE is used as a cross-coupling reagent in the synthesis of complex molecules. Its reactivity allows for the formation of new chemical bonds, facilitating the creation of diverse molecular structures with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 69404-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,0 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69404-97:
(7*6)+(6*9)+(5*4)+(4*0)+(3*4)+(2*9)+(1*7)=153
153 % 10 = 3
So 69404-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H22O2Si/c1-9(12)8-10(2)13-14(6,7)11(3,4)5/h8H,1-7H3/b10-8+
69404-97-3Relevant articles and documents
A CLASS OF NEW SILYLATING REAGENTS. I. A MILD METHOD FOR INTRODUCTION OF THE TERT-BUTYLDIMETHYLSILYL GROUP.
Veysoglu, Tarik,Mitscher, Lester A.
, p. 1299 - 1302 (1981)
t-Butyldimethylsilyl enol ethers of pentane-2,4-dione and methyl acetoacetate react rapidly at room temperature to give high isolated yields of the t-butydimethylsilyl ethers of a variety of alcohols.