909186-19-2 Usage
Description
(4-chloro-2-fluorobenzyloxy)(tert-butyl)dimethylsilane is an organosilicon compound characterized by the presence of a benzyl ether and tert-butyl groups attached to a silicon atom. It also features a chlorine and fluorine substituent on the benzene ring, which contributes to its unique structure and reactivity. (4-chloro-2-fluorobenzyloxy)(tert-butyl)dimethylsilane is known for its versatility in organic synthesis and its ability to serve as a protecting group for alcohols in various organic reactions.
Uses
Used in Organic Synthesis:
(4-chloro-2-fluorobenzyloxy)(tert-butyl)dimethylsilane is used as a building block in the synthesis of a wide range of organic compounds. Its unique structure allows for the creation of diverse molecules with potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science.
Used as a Protecting Group for Alcohols:
In the field of organic chemistry, (4-chloro-2-fluorobenzyloxy)(tert-butyl)dimethylsilane serves as an effective protecting group for alcohols during reactions. This function is crucial for preventing unwanted side reactions and ensuring the selective formation of the desired product.
Used in the Introduction of Silicon-Containing Groups:
The presence of the silicon atom in (4-chloro-2-fluorobenzyloxy)(tert-butyl)dimethylsilane makes it a valuable reagent for introducing silicon-containing groups into organic molecules. This can be particularly useful in the development of new materials with enhanced properties, such as improved thermal stability or increased bioavailability in pharmaceutical applications.
Used in Pharmaceutical Industry:
(4-chloro-2-fluorobenzyloxy)(tert-butyl)dimethylsilane is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity enable the development of new drugs with improved efficacy and selectivity.
Used in Materials Science:
In the field of materials science, (4-chloro-2-fluorobenzyloxy)(tert-butyl)dimethylsilane is used as a precursor for the development of novel materials with specific properties, such as enhanced thermal stability, chemical resistance, or optical characteristics. These materials can find applications in various industries, including electronics, aerospace, and automotive.
Check Digit Verification of cas no
The CAS Registry Mumber 909186-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,1,8 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 909186-19:
(8*9)+(7*0)+(6*9)+(5*1)+(4*8)+(3*6)+(2*1)+(1*9)=192
192 % 10 = 2
So 909186-19-2 is a valid CAS Registry Number.
909186-19-2Relevant articles and documents
3-Amino-7-phthalazinylbenzoisoxazoles as a novel class of potent, selective, and orally available inhibitors of p38α mitogen-activated protein kinase
Pettus, Liping H.,Xu, Shimin,Cao, Guo-Qiang,Chakrabarti, Partha P.,Rzasa, Robert M.,Sham, Kelvin,Wurz, Ryan P.,Zhang, Dawei,Middleton, Scott,Henkle, Bradley,Plant, Matthew H.,Saris, Christiaan J. M.,Sherman, Lisa,Lu, Min Wong,Powers, David A.,Tudor, Yanyan,Yu, Violeta,Lee, Matthew R.,Syed, Rashid,Hsieh, Faye,Tasker, Andrew S.
experimental part, p. 6280 - 6292 (2009/10/09)
The p38 mitogen-activated protein kinase (MAPK) is a central signaling molecule in many proinflammatory pathways, regulating the cellular response to a multitude of external stimuli including heat, ultraviolet radiation, osmotic shock, and a variety of cy
