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Diphenyl(o-tolyl)silanol is an organosilicon compound with the chemical formula C19H18OSi. It is a colorless to pale yellow liquid and is characterized by the presence of two phenyl groups and an o-tolyl group (a methyl-substituted phenyl group) attached to a silicon atom, which is also bonded to a hydroxyl group. diphenyl(o-tolyl)silanol is used in the synthesis of various organosilicon materials, such as silicones and silanes, and can be employed as a coupling agent or a cross-linking agent in the production of polymers and resins. Due to its unique structure, diphenyl(o-tolyl)silanol exhibits interesting properties, such as thermal stability and reactivity with various functional groups, making it a valuable intermediate in organic synthesis and material science.

736-71-0

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736-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 736-71-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 736-71:
(5*7)+(4*3)+(3*6)+(2*7)+(1*1)=80
80 % 10 = 0
So 736-71-0 is a valid CAS Registry Number.

736-71-0Downstream Products

736-71-0Relevant academic research and scientific papers

Selective Electrochemical Hydrolysis of Hydrosilanes to Silanols via Anodically Generated Silyl Cations

Liang, Hao,Wang, Lu-Jun,Ji, Yun-Xing,Wang, Han,Zhang, Bo

supporting information, p. 1839 - 1844 (2020/12/01)

The first electrochemical hydrolysis of hydrosilanes to silanols under mild and neutral reaction conditions is reported. The practical protocol employs commercially available and cheap NHPI as a hydrogen-atom transfer (HAT) mediator and operates at room temperature with high selectivity, leading to various valuable silanols in moderate to good yields. Notably, this electrochemical method exhibits a broad substrate scope and high functional-group compatibility, and it is applicable to late-stage functionalization of complex molecules. Preliminary mechanistic studies suggest that the reaction appears to proceed through a nucleophilic substitution reaction of an electrogenerated silyl cation with H2O.

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