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Tris(trans-1,2-cyclopropanediyldimethylene) diborate, also known as tris(1,2-cyclohexanediyl)diborate or commonly referred to as "TBD", is a boron-containing compound with the chemical formula C18H30B2O6. It is a colorless, crystalline solid that is highly soluble in organic solvents. TBD is widely used as a Lewis acid catalyst in various organic reactions, particularly in the formation of carbon-carbon bonds and in the synthesis of complex organic molecules. It is known for its stability, high catalytic activity, and ability to form stable complexes with a variety of substrates. The compound's structure features three cyclopropane rings bridging two boron atoms, which contributes to its unique reactivity and selectivity in catalytic processes.

86022-60-8

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86022-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86022-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86022-60:
(7*8)+(6*6)+(5*0)+(4*2)+(3*2)+(2*6)+(1*0)=118
118 % 10 = 8
So 86022-60-8 is a valid CAS Registry Number.

86022-60-8Downstream Products

86022-60-8Relevant academic research and scientific papers

Molecular structure and vibrational circular dichroism of tris(trans-1,2-cyclopropanediyldimethylene) diborate, a new, stable bridged borate ester

Heintz,Freeman, Wade A.,Keiderling

, p. 2319 - 2324 (2008/10/08)

In this paper are presented the preparation, properties, crystal structure, and infrared, Raman, and vibrational circular dichroism (VCD) spectra of the title compound, a novel triply bridged diborate ester, B(OCH2C3H4CH2O)3B. This compound is unusually resistant to hydrolysis and crystallizes in the hexagonal system, space group P63, with a = 11.294 (3) ?, c = 7.644 (4) ?, and Z = 2. Its structure was solved by direct methods and refined to a conventional R factor of 0.074 for 1290 unique data. The molecule has C3 symmetry with the cyclopropane bridges imposing helicity. The IR, Raman, and VCD spectra can be correlated to those of previously studied disubstituted cyclopropanes. Very large VCD signals were observed which appear to arise from coupling of the symmetry-related parts of the molecule.

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