10487-11-3 Usage
Uses
Used in Pharmaceutical Industry:
1,1,1,7,7,7-HEXAFLUORO-2,6-DIHYDROXY-2,6-BIS(TRIFLUOROMETHYLHEPTAN-4-ONE) is used as a building block for the synthesis of pharmaceuticals due to its ability to contribute to the development of novel drug molecules with enhanced properties.
Used in Agrochemical Industry:
In the agrochemical sector, 1,1,1,7,7,7-HEXAFLUORO-2,6-DIHYDROXY-2,6-BIS(TRIFLUOROMETHYLHEPTAN-4-ONE) serves as a key component in the creation of new agrochemicals, potentially improving the effectiveness and selectivity of pesticides and other agricultural chemicals.
Used in Specialty Chemicals Synthesis:
1,1,1,7,7,7-HEXAFLUORO-2,6-DIHYDROXY-2,6-BIS(TRIFLUOROMETHYLHEPTAN-4-ONE) is utilized as a building block in the synthesis of specialty chemicals, where its unique structure can impart specific characteristics to the final products, catering to niche applications.
Used as a Reagent in Organic Synthesis:
1,1,1,7,7,7-HEXAFLUORO-2,6-DIHYDROXY-2,6-BIS(TRIFLUOROMETHYLHEPTAN-4-ONE) is employed as a reagent in organic synthesis, where its stability and reactivity can facilitate targeted chemical reactions, leading to the formation of desired organic compounds.
Used as a Solvent in Various Industries:
Due to its unique properties, 1,1,1,7,7,7-HEXAFLUORO-2,6-DIHYDROXY-2,6-BIS(TRIFLUOROMETHYLHEPTAN-4-ONE) is also used as a solvent across different industries, providing a medium for chemical reactions to occur, particularly in processes that require a stable and inert environment.
Check Digit Verification of cas no
The CAS Registry Mumber 10487-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10487-11:
(7*1)+(6*0)+(5*4)+(4*8)+(3*7)+(2*1)+(1*1)=83
83 % 10 = 3
So 10487-11-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F12O3/c10-6(11,12)4(23,7(13,14)15)1-3(22)2-5(24,8(16,17)18)9(19,20)21/h23-24H,1-2H2
10487-11-3Relevant academic research and scientific papers
The cross-aldol reaction of hexafluoroacetone (HFA) with ketones catalyzed by an acid
Komata, Takeo,Matsunaga, Kei,Hirotsu, Yoshiki,Akiba, Shinya,Ogura, Katsuyuki
, p. 902 - 909 (2008/03/14)
The cross-aldol reactions of hexafluoroacetone (HFA) and ketones using an acid catalyst are reported. When concentrated sulfuric acid was employed as the catalyst, HFA reacted regioselectively with various ketones at 50-100 °C to give the aldol adducts (6) in good yields. The reaction is initiated by an acid-catalyzed transformation of the ketone into the corresponding enol that reacts with HFA. The obtained adducts (6) can be reduced with hydrogen under a Ru/C catalyst to lead to the corresponding fluorine-containing diols (13).
