107149-55-3 Usage
Uses
Used in the Synthesis of Organosilicon Compounds:
T-BUTYLDIETHYLCHLOROSILANE is used as a reagent for the synthesis of various organosilicon compounds, leveraging its reactivity to form a wide range of silicon-containing materials.
Used as a Protecting Agent in Organic Chemistry:
T-BUTYLDIETHYLCHLOROSILANE is used as a protecting agent for hydroxyl groups, which is crucial in organic synthesis to prevent unwanted reactions from occurring at the hydroxyl sites.
Used in Materials Science:
T-BUTYLDIETHYLCHLOROSILANE is used as a precursor for the functionalization of surfaces, contributing to the development of advanced materials with tailored properties.
Used in the Semiconductor Industry:
In the semiconductor industry, T-BUTYLDIETHYLCHLOROSILANE is utilized for surface modification to enhance the performance of semiconductor devices.
Safety Precautions:
Due to its highly flammable and corrosive nature, T-BUTYLDIETHYLCHLOROSILANE should be handled and stored with appropriate safety measures to prevent accidents and ensure the well-being of individuals and the integrity of the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 107149-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,4 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107149-55:
(8*1)+(7*0)+(6*7)+(5*1)+(4*4)+(3*9)+(2*5)+(1*5)=113
113 % 10 = 3
So 107149-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H19ClSi/c1-6-10(9,7-2)8(3,4)5/h6-7H2,1-5H3
107149-55-3Relevant academic research and scientific papers
Steroidal Silicon Side-Chain Analogues as Potential Antifertility Agents
Peters, Richard H.,Crowe, David F.,Tanabe, Masato,Avery, Mitchell A.,Chong, Wesley K. M.
, p. 646 - 652 (2007/10/02)
A number of silicon-substituted analogues of ethynylestradiol that exhibit modified and enhanced biological activities have been synthesized.Particularly noteworthy are a group of estradiol analogues that exhibit high antifertility potency and markedly reduced estrogenic activity.The best compounds synthesized are 17α-estradiol (5) and 17α-estradiol (33), which show a separation of antifertility from estrogenic activity in the rat.The results of structure-activity studies indicate a good correlation between the observed biological activities and the calculated van der Waals volumes of the three variable silicon substituents.
