107149-56-4 Usage
Uses
Used in Pharmaceutical Industry:
DIETHYLISOPROPYLSILYL CHLORIDE is used as a reagent for the synthesis of complex organic compounds, particularly for the protection of hydroxyl groups in organic molecules. It is utilized in the development of new pharmaceuticals, enhancing the efficiency and selectivity of chemical reactions.
Used in Agrochemical Industry:
In the agrochemical sector, DIETHYLISOPROPYLSILYL CHLORIDE is used as a reagent for the synthesis of complex organic compounds, which are essential in the development of new agrochemicals. Its application aids in the protection of functional groups, facilitating the creation of more effective and targeted agrochemical products.
Used in Organic Synthesis:
DIETHYLISOPROPYLSILYL CHLORIDE is used as a reagent for introducing the diethylisopropylsilyl (DES) protecting group into various functional groups in organic synthesis. This application is crucial for the selective protection and deprotection of reactive sites in organic molecules, allowing for more controlled and precise chemical reactions.
Used in the Protection of Hydroxyl Groups:
DIETHYLISOPROPYLSILYL CHLORIDE is used as a protecting agent for hydroxyl groups in organic molecules. This is particularly important in complex organic synthesis, where the protection of hydroxyl groups can prevent unwanted side reactions and improve the overall yield and purity of the desired product.
Check Digit Verification of cas no
The CAS Registry Mumber 107149-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,4 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107149-56:
(8*1)+(7*0)+(6*7)+(5*1)+(4*4)+(3*9)+(2*5)+(1*6)=114
114 % 10 = 4
So 107149-56-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H17ClSi/c1-5-9(8,6-2)7(3)4/h7H,5-6H2,1-4H3
107149-56-4Relevant 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.
