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1,3-bis(trimethylsilyl)-2,4-bis{bis(trimethylsilyl)amino}-1,3-diazadiboretane is a complex organosilicon compound characterized by its unique structure and properties. This molecule consists of a 1,3-diazadiboretane core, which is a five-membered ring containing two nitrogen atoms and one boron atom. The boron atom is bonded to two trimethylsilyl groups, while the nitrogen atoms are each bonded to a bis(trimethylsilyl)amino group. The presence of multiple trimethylsilyl groups in the molecule contributes to its stability and reactivity. 1,3-bis(trimethylsilyl)-2,4-bis{bis(trimethylsilyl)amino}-1,3-diazadiboretane has potential applications in various fields, including materials science, pharmaceuticals, and chemical synthesis, due to its ability to form stable complexes with transition metals and its potential as a ligand in coordination chemistry.

6689-36-7

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6689-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6689-36-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,8 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6689-36:
(6*6)+(5*6)+(4*8)+(3*9)+(2*3)+(1*6)=137
137 % 10 = 7
So 6689-36-7 is a valid CAS Registry Number.

6689-36-7Downstream Products

6689-36-7Relevant academic research and scientific papers

Reactivity of Terminal Iron Borylenes and Bis(borylenes) with Carbodiimides: Cycloaddition, Metathesis, Insertion and C?H Activation Pathways

Matler, Alexander,Arrowsmith, Merle,Schorr, Fabian,Hermann, Alexander,Hofmann, Alexander,Lenczyk, Carsten,Braunschweig, Holger

, p. 4619 - 4631 (2021/10/04)

The reactions of carbodiimides with the iron arylborylene complex [Fe=BDur(CO)3(PMe3)] (Dur=2,3,5,6-Me4C6H) and the iron bis(borylene) complex [Fe{=BDur}{=BN(SiMe3)2}(CO)3] yield a wide variety of temperature-dependent products, including known FeBNC and novel FeBNB metallacycles, complexes of N-heterocyclic boracarbene and spiro-boracarbene ligands and a unique 1,3,2,4-diazadiborolyl pianostool complex, characterized by NMR spectroscopy and X-ray crystallography. The product distributions can be rationalized by considering sequences of cycloaddition, metathesis, insertion, and C?H activation pathways mainly governed by sterics.

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