56253-60-2 Usage
Uses
Used in Organic Synthesis:
(Phenylselenomethyl)trimethylsilane is utilized as a reagent in organic synthesis for its distinctive properties that facilitate various chemical reactions. Its presence can influence the outcome of reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (Phenylselenomethyl)trimethylsilane is used as a building block for the development of new drugs. Its selenium-containing structure can contribute to the creation of novel therapeutic agents with potential applications in medicine.
Used in Chemical Research:
(Phenylselenomethyl)trimethylsilane is employed as a research tool in chemical laboratories. Its unique properties make it an interesting subject for studies aimed at understanding the behavior of organosilicon and organoselenium compounds in different reaction conditions.
Used in Material Science:
In the field of material science, (Phenylselenomethyl)trimethylsilane is used as a precursor for the development of new materials with specific properties. Its incorporation into materials can lead to the creation of novel compounds with applications in various industries, such as electronics or coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 56253-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,5 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56253-60:
(7*5)+(6*6)+(5*2)+(4*5)+(3*3)+(2*6)+(1*0)=122
122 % 10 = 2
So 56253-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H16SeSi/c1-12(2,3)9-11-10-7-5-4-6-8-10/h4-8H,9H2,1-3H3
56253-60-2Relevant academic research and scientific papers
1-(organoselanyl)perfluoroalkanols: A stable and efficient precursor for organoselenols
Yamamoto, Terahisa,Moriura, Eri,Sawa, Arisa,Yoshimatsu, Mitsuhiro
scheme or table, p. 1046 - 1047 (2009/12/03)
The 1-(organoselanyl)perfluoroalkanols 1, 3, 4, and 10 were successfully prepared and reactions with hexanoyl chlorides to produce the corresponding esters 5, 7, and 8, accompanied by the selenoesters 6 were conducted. The DBU-mediated alkylations of the heptafluorobutanols 4, 10, and the α-p-nitro-benzoate 2 with alkyl halides easily provided alkyl phenyl selenides 9a-9i and 11a-11c in good to high yields. Copyright
THE REACTIONS OF LITHIOBISPHENYLSELENOMETHANE WITH CHLOROMETHYLTRIMETHYLSILANE AND IODOMETHYLTRIMETHYLSTANNANE: NOVEL 1,1 -AND 1,2-ELIMINATION REACTIONS IN ORGANOSELENIUM/ORGANOTIN CHEMISTRY
Sarkar, Tarun K.,Satapathi, Tushar K.
, p. 3333 - 3334 (2007/10/02)
Anomalous and unprecedented 1,1- and 1,2-elimination reactions are reported in the alkylation of lithiobisphenylselenomethane 4 with chloromethyltrimethylsilane and iodomethyltrimethylstannane.
TRANSFORMATION OF α-PHENYLSELENOKETONES TO ALLYLIC SELENIDES VIA MIGRATION OF THE PHENYLSELENO GROUP
Nishiyama, Hisao,Itagaki, Kazuyoshi,Osaka, Noriyuki,Itoh, Kenji
, p. 4103 - 4106 (2007/10/02)
α-Phenylselenoketones were readily converted to the allylic selenides by treatment with trimethylsilylmethyllithium and subsequent reaction with tin(II)chloride via a facile migration of the phenylseleno group in course of the reaction.
