867-97-0

Usage

Uses

Used in Organic Chemistry:
Boranetriamine, N,N,N',N',N'',N''-hexaethylis used as a key intermediate in the synthesis of complex organic molecules. Its readiness to react with a broad spectrum of organic compounds facilitates the creation of intricate structures in organic chemistry.
Used in Material Science:
In the field of material science, Boranetriamine, N,N,N',N',N'',N''-hexaethylis utilized for the development of advanced polymers. Its unique properties contribute to the enhancement of material characteristics, leading to improved performance in various applications.
Used in Pharmaceutical Development:
Boranetriamine, N,N,N',N',N'',N''-hexaethylalso holds potential in the pharmaceutical industry. It serves as a precursor for the synthesis of new pharmaceutical compounds, potentially leading to the discovery of novel drugs and therapeutic agents.
Used in Research Applications:
Due to its reactivity and the ability to form organoboron compounds, Boranetriamine, N,N,N',N',N'',N''-hexaethylis employed in research settings to explore new chemical reactions and investigate the properties of boron-containing compounds. This research can lead to advancements in various scientific disciplines.

Upstream product

• 1113-31-1 dichlorodimethylaminoborane 
• 75-04-7 ethylamine 
• 856314-21-1 dimethyl-amine; compound with boron chloride 
• 124-40-3 dimethyl amine 
• 79812-14-9 Bis(diethylamino)(trimethylstannyl)boran 
• 75-65-0 tert-butyl alcohol 
• 868-25-7 bis(diethylamino)boron chloride 
• 925-90-6 ethylmagnesium bromide 
• 591-51-5 phenyllithium 
• 109-89-7 diethylamine 

Downstream Products

• 1223-06-9 m-CH₃C₆H₄NHB{N(C₂H₅)2}2 
• 40347-74-8 Bis-benzhydrylidenamino-diethylamino-boran 
• 24388-27-0 2-(diethylamino)-1,3,2-dioxaborolane 
• 107697-49-4 (BN(C₆H₅)CH₂CH₂N)3 
• 25031-73-6 1,3-dimethyl-2-diethylamino-1,3,2-diazaboracyclohexane 
• 84942-16-5 Tris-(diphenylamino)-boran 
• 7397-43-5 tri-(tert-butyl)borate 
• 4023-39-6 diethyl-diethylamino-borane 
• 660-68-4 diethyl amine hydrochloride 
• 868-30-4 Diethylaminodichloroborane 
• 1234-11-3 (2-CH₃C₆H₄NH)2BN(C₂H₅)2 
• 1217-78-3 Anilino-bis-diaethylamino-bor 

Relevant academic research and scientific papers

Using Ylide Functionalization to Stabilize Boron Cations

The metalated ylide YNa [Y=(Ph3PCSO2Tol)?] was employed as X,L-donor ligand for the preparation of a series of boron cations. Treatment of the bis-ylide functionalized borane Y2BH with different trityl salts or B(C6F5)3 for hydride abstraction readily results in the formation of the bis-ylide functionalized boron cation [Y?B?Y]+ (2). The high donor capacity of the ylide ligands allowed the isolation of the cationic species and its characterization in solution as well as in solid state. DFT calculations demonstrate that the cation is efficiently stabilized through electrostatic effects as well as π-donation from the ylide ligands, which results in its high stability. Despite the high stability of 2 [Y?B?Y]+ serves as viable source for the preparation of further borenium cations of type Y2B+←LB by addition of Lewis bases such as amines and amides. Primary and secondary amines react to tris(amino)boranes via N?H activation across the B?C bond.

Preparation of some organo-bis(diisopropylamino)boranes and their application to the synthesis of oxazaborolidines

The reactivity of ClB(NEt2)2 and ClB(NiPr2)2 towards organomagnesium or organolithium derivatives was studied.ClB(NiPr2)2 proved to be an excellent reagent for the preparation of pure boronic derivatives RB(NiPr2)2, which

Metall-Bor-Verbindungen, 13. Zur Synthese und Reaktivitaet einiger (Trimethylstannyl)borane

The preparation of some amino(trimethylstannyl)boranes and their chemical properties are described.With Me3SnLi (Me = CH3) as a reagent only the synthesis of Me3SnB(NR2)2 (1a, b), Me3SnBCl(NR2) (2a, b), and (Me3Sn)2BNR2 (3b) was achieved.The stannylboranes Me3SnB(NR2)2 show astonishing thermal stability.Their Sn - B bonds are broken by hydrogen, the halogens, and chalcogens as well as by alcohols.HCl cleaves the B - N bond.