145251-89-4 Usage
Uses
Used in Organic Synthesis:
2-(TRIISOPROPYLSILYL)-1 3-DITHIANE 97 is used as a reagent for the protection of aldehydes and ketones during the synthesis of various organic compounds. Its selective protection of carbonyl groups is crucial in preventing unwanted side reactions, thereby enhancing the yield and purity of the target molecules.
Used in Chemical Research:
In the realm of chemical research, 2-(TRIISOPROPYLSILYL)-1 3-DITHIANE 97 is employed as a valuable tool for the exploration of new reaction pathways and the development of innovative synthetic strategies. Its high purity and reactivity make it an essential component in the experimental setups of many research projects.
Used in Pharmaceutical Industry:
2-(TRIISOPROPYLSILYL)-1 3-DITHIANE 97 is used as a key intermediate in the synthesis of pharmaceutical compounds. Its role in protecting sensitive functional groups during the synthesis process is vital for the production of complex drug molecules with high purity and efficacy.
Used in Material Science:
In material science, 2-(TRIISOPROPYLSILYL)-1 3-DITHIANE 97 is utilized in the synthesis of novel materials with unique properties. Its ability to protect carbonyl groups during the formation of polymers and other complex structures contributes to the development of advanced materials with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 145251-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,2,5 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 145251-89:
(8*1)+(7*4)+(6*5)+(5*2)+(4*5)+(3*1)+(2*8)+(1*9)=124
124 % 10 = 4
So 145251-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H27ClSi4/c1-11(2,3)14(10,12(4,5)6)13(7,8)9/h1-9H3
145251-89-4Relevant academic research and scientific papers
Enantioselective preparation of 2-substituted-1,3-dithiane 1-oxides using modified Sharpless sulphoxidation procedures
Page, Philip C. Bulman,Wilkes, Robin D.,Namwindwa, Ernest S.,Witty, Michael J.
, p. 2125 - 2154 (2007/10/03)
Enantioselective sulphoxidation of a wide range of 2-substituted-1,3-diathianes has been carried out using modified Sharpless conditions to furnish the corresponding sulphoxides in optically enriched form. Deacylation of 2-acyl-1,3-dithiane 1-oxide deriva
