603045-12-1 Usage
Description
(S)-(but-3-yn-2-yloxy)(tert-butyl)diphenylsilane is a silane compound with a molecular formula C22H25OSi. It is composed of a silicon atom bonded to two phenyl groups, a tert-butyl group, and a but-3-yn-2-yloxy group in an (S) configuration. (S)-(but-3-yn-2-yloxy)(tert-butyl)diphenylsilane is characterized by its unique structure, which includes the diphenylsilane group, the tert-butyl group, and the but-3-yn-2-yloxy group. The presence of these functional groups suggests that this compound may have potential applications in various fields, particularly in organic chemistry and materials science.
Uses
Used in Organic Synthesis:
(S)-(but-3-yn-2-yloxy)(tert-butyl)diphenylsilane is used as a precursor in the synthesis of organosilicon compounds. The diphenylsilane group in this compound makes it a valuable building block for the creation of more complex molecules, which can be further utilized in various chemical reactions and processes.
Used in Materials Science:
In the field of materials science, (S)-(but-3-yn-2-yloxy)(tert-butyl)diphenylsilane can be used as a building block for the development of new materials with specific properties. (S)-(but-3-yn-2-yloxy)(tert-butyl)diphenylsilane's unique structure, including the tert-butyl group and the but-3-yn-2-yloxy group, may contribute to the enhancement of certain material characteristics, such as stability, reactivity, or compatibility with other components.
Used in Pharmaceutical Industry:
(S)-(but-3-yn-2-yloxy)(tert-butyl)diphenylsilane may also find applications in the pharmaceutical industry, where it can be used as an intermediate in the synthesis of various drugs and drug candidates. (S)-(but-3-yn-2-yloxy)(tert-butyl)diphenylsilane's unique structure and functional groups can be exploited to design and develop novel therapeutic agents with improved efficacy and selectivity.
Used in Chemical Research:
In the realm of chemical research, (S)-(but-3-yn-2-yloxy)(tert-butyl)diphenylsilane can serve as a valuable tool for studying the properties and reactivity of silane compounds. Researchers can use this compound to explore new reaction pathways, develop innovative synthetic strategies, and gain insights into the fundamental principles governing the behavior of organosilicon compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 603045-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,3,0,4 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 603045-12:
(8*6)+(7*0)+(6*3)+(5*0)+(4*4)+(3*5)+(2*1)+(1*2)=101
101 % 10 = 1
So 603045-12-1 is a valid CAS Registry Number.
603045-12-1Relevant articles and documents
The synthesis of unnatural α-alkyl- And α-aryl-substituted serine derivatives
Narczyk, Aleksandra,Stecko, Sebastian
supporting information, p. 1204 - 1213 (2020/02/22)
The synthesis of α-aryl- and α-alkyl-substituted serine derivatives via [3,3]-sigmatropic rearrangement of allyl carbamates as a key step is reported. Allyl carbamates were obtained from the corresponding allyl alcohols. The former were prepared through three approaches. Aryl-substituted ones were synthesized via the Stille coupling reaction of aryl iodides with enantiomerically enriched vinyl stannanes. Conversely, alkyl-substituted allyl alcohols were prepared by an analogous strategy involving the Negishi coupling reaction of enantiomerically enriched vinyl iodides or by enzymatic kineric resolution of the corresponding racemic alcohols.
