108613-97-4 Usage
Uses
Used in Organic Synthesis:
((4-(4-Propyl-2,6,7-trioxabicyclo(2.2.2)oct-1-yl)phenyl)ethynyl)trimethylsilane is used as a synthetic building block for the creation of more complex organic molecules. Its unique structure allows for various chemical reactions, enabling the synthesis of new compounds with potential applications in different industries.
Used in Materials Science:
In the field of materials science, ((4-(4-Propyl-2,6,7-trioxabicyclo(2.2.2)oct-1-yl)phenyl)ethynyl)trimethylsilane can be utilized as a component in the development of advanced materials. Its diverse structure may contribute to the creation of materials with specific properties, such as improved stability, reactivity, or selectivity.
Used in Pharmaceutical Research:
((4-(4-Propyl-2,6,7-trioxabicyclo(2.2.2)oct-1-yl)phenyl)ethynyl)trimethylsilane may also be employed in pharmaceutical research as a potential candidate for drug development. Its complex structure could be harnessed to design new drugs with specific therapeutic effects or to improve the delivery and efficacy of existing medications.
Check Digit Verification of cas no
The CAS Registry Mumber 108613-97-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,1 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108613-97:
(8*1)+(7*0)+(6*8)+(5*6)+(4*1)+(3*3)+(2*9)+(1*7)=124
124 % 10 = 4
So 108613-97-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H26O3Si/c1-5-11-18-13-20-19(21-14-18,22-15-18)17-8-6-16(7-9-17)10-12-23(2,3)4/h6-9H,5,11,13-15H2,1-4H3
108613-97-4Relevant academic research and scientific papers
Improvements relating to pesticides
-
, (2008/06/13)
Bicyclo-octane pesticides have the formula where Z is CH2CH2, CH2O, CH2S, -COCH2 or CH(OR8)CH2 where R8 is H, alkyl, acyl or carbamoyl; Y and Y1 are O or S(O)mwhere m is 0, 1 or 2; R is a specified substituted or unsubstituted aliphatic or cycloaliphatic hydrocarbon groups or a phenyl group, R1 and R3 are H, or specified substituted or unsubstituted aliphatic hydrocarbon groups or R1 is a carboalkoxy, cyano or gem dimethyl group when R3 is H or R and R1, together with the carbon atoms to which they are attached form a carbocyclic ring; and R2 is a phenyl group substituted at position 4 by -(C≡C)nR5 and optionally at other positions by specified substituents where n is 1 or 2 and R5 is I, H, alkyl optionally substituted, carboalkoxy, or a trisubstituted tin or trisubstituted silicon group. Various methods of synthesis are given.
Selective catalytic hydrogenation of an olefin moiety in the presence of a terminal alkyne function
Palmer,Casida
, p. 2857 - 2860 (2007/10/02)
Protection of a terminal alkyne as a (trimethyl- or tri-isopropylsilyl)alkyne permits selective catalytic hydrogenation of a mono- or disubstituted olefin moiety without reducing the alkyne function.
