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2-butoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a complex organic compound with the chemical formula C9H19BO4. It is a colorless liquid that is soluble in organic solvents. 2-butoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a derivative of 1,3,2-dioxaborolane, which is a boron-containing heterocycle. It is used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, a type of reaction used to form carbon-carbon bonds. The butoxy group in 2-butoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane plays a role in the reaction mechanism, facilitating the transfer of a boron group to an organic substrate, which is crucial for the formation of the desired product. Its stability and reactivity make it a valuable tool in the synthesis of various organic compounds, including pharmaceuticals and specialty chemicals.

1135-07-5

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1135-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1135-07-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1135-07:
(6*1)+(5*1)+(4*3)+(3*5)+(2*0)+(1*7)=45
45 % 10 = 5
So 1135-07-5 is a valid CAS Registry Number.

1135-07-5Downstream Products

1135-07-5Relevant academic research and scientific papers

Readily available lithium compounds as catalysts for the hydroboration of carbodiimides and esters

Bisai, Milan Kumar,Das, Tamal,Gour, Kritika,Sen, Sakya S.,Vanka, Kumar

, (2021)

Selective and efficient hydroboration of esters and carbodiimides to alcohols and amines by two well-defined and readily accessible lithium complexes, 2,6-di-tert-butyl phenolate lithium (1a) and 1,1’-dilithioferrocene (1b) are described. A range of aliphatic, aromatic, and cyclic esters with various functional groups were selectively converted into the corresponding boronate esters. Similarly, the single hydroboration of carbodiimides with aliphatic and aromatic substituents on the nitrogen atoms was studied. A possible mechanistic pathway of the hydroboration of carbodiimides with HBpin has been proposed using NMR studies and DFT calculations. These reactions are convenient alternatives to stoichiometric hydride reduction or hydrogenation. The employing of lithium complexes is also significant, because of the need to find cheap and green alternatives to noble metal complexes.

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