701-35-9 Usage
Uses
Used in Chemical Synthesis:
P-TOLYLTRICHLOROSILANE is used as an intermediate for the production of 3-(p-Methylphenyl)cyclohexanon, a compound with potential applications in the pharmaceutical and chemical industries. Its unique chemical structure allows for further functionalization and modification, making it a valuable building block in the synthesis of complex organic molecules.
Used in the Pharmaceutical Industry:
P-TOLYLTRICHLOROSILANE is used as a synthetic building block for the development of new pharmaceutical compounds. Its reactivity and compatibility with various functional groups make it a promising candidate for the creation of novel drug molecules with potential therapeutic applications.
Used in the Chemical Industry:
P-TOLYLTRICHLOROSILANE is used as a versatile reagent in the chemical industry for the synthesis of a wide range of organic compounds. Its ability to undergo various chemical reactions, such as substitution, addition, and condensation, makes it a valuable asset in the development of new materials and products.
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 701-35-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 701-35:
(5*7)+(4*0)+(3*1)+(2*3)+(1*5)=49
49 % 10 = 9
So 701-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7Cl3Si/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3
701-35-9Relevant academic research and scientific papers
Asymmetric Synthesis of Silicon-Stereogenic Silanes by Copper-Catalyzed Desymmetrizing Protoboration of Vinylsilanes
Li, Yanfei,Wang, Ying,Xiong, Tao,Zhang, Ge,Zhang, Qian
supporting information, p. 11927 - 11931 (2020/05/22)
The catalytic asymmetric creation of silanes with silicon stereocenters is a long-sought but underdeveloped topic, and only a handful of examples have been reported. Moreover, the construction of chiral silanes containing (more than) two stereocenters is a more arduous task and remains unexploited. We herein report an unprecedented copper-catalyzed desymmetrizing protoboration of divinyl-substituted silanes with bis(pinacolato)diboron (B2pin2). This method enables the facile preparation of an array of enantiomerically enriched boronate-substituted organosilanes bearing contiguous silicon and carbon stereocenters with exclusive regioselectivity and generally excellent diastereo- and enantioselectivity.
