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Tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methane is a complex organic compound with the chemical formula C18H33B3O6. It is a colorless, crystalline solid that is soluble in organic solvents. tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methane is widely used in organic synthesis, particularly in the field of cross-coupling reactions, as a boron-based reagent. It is known for its stability and ability to form strong carbon-boron bonds, which can be further transformed into carbon-carbon or carbon-heteroatom bonds under the influence of a suitable catalyst. The compound's structure features a central methane molecule with three 1,3,2-dioxaborolane moieties attached, each of which contributes to the reactivity and selectivity of the molecule in various chemical transformations.

29173-23-7

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29173-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29173-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,7 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29173-23:
(7*2)+(6*9)+(5*1)+(4*7)+(3*3)+(2*2)+(1*3)=117
117 % 10 = 7
So 29173-23-7 is a valid CAS Registry Number.

29173-23-7Downstream Products

29173-23-7Relevant academic research and scientific papers

Fully Borylated Methane and Ethane by Ruthenium-Mediated Cleavage and Coupling of CO

Batsanov, Andrei S.,Cabeza, Javier A.,Crestani, Marco G.,Fructos, Manuel R.,García-álvarez, Pablo,Gille, Marie,Lin, Zhenyang,Marder, Todd B.

supporting information, p. 4707 - 4710 (2016/04/19)

Many transition-metal complexes and some metal-free compounds are able to bind carbon monoxide, a molecule which has the strongest chemical bond in nature. However, very few of them have been shown to induce the cleavage of its C-O bond and even fewer are those that are able to transform CO into organic reagents with potential in organic synthesis. This work shows that bis(pinacolato)diboron, B2pin2, reacts with ruthenium carbonyl to give metallic complexes containing borylmethylidyne (CBpin) and diborylethyne (pinBC≡CBpin) ligands and also metal-free perborylated C1 and C2 products, such as C(Bpin)4 and C2(Bpin)6, respectively, which have great potential as building blocks for Suzuki-Miyaura cross-coupling and other reactions. The use of 13CO-enriched ruthenium carbonyl has demonstrated that the boron-bound carbon atoms of all of these reaction products arise from CO ligands.

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