867-97-0

Basic information

• Product Name: BoranetriaMine, N,N,N',N',N'',N''-hexaethyl-
• Synonyms: BoranetriaMine, N,N,N',N',N'',N''-hexaethyl-;N,N,N',N',N'',N''-hexaethylboranetriamine
• CAS NO: 867-97-0
• Molecular Formula: C₁₂H₃₀BN₃
• Molecular Weight: 227.1977
• Mol File: 867-97-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BoranetriaMine, N,N,N',N',N'',N''-hexaethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: BoranetriaMine, N,N,N',N',N'',N''-hexaethyl-(867-97-0)
• EPA Substance Registry System: BoranetriaMine, N,N,N',N',N'',N''-hexaethyl-(867-97-0)

Safety Data

• Hazardous Substances Data: 867-97-0(Hazardous Substances Data)

Usage

General Description

Boranetriamine, N,N,N',N',N'',N''-hexaethyl- is a chemical compound that consists of a boron atom and six ethyl groups. It is primarily used as a building block in the synthesis of other organoboron compounds, which have numerous industrial and research applications. Boranetriamine, N,N,N',N',N'',N''-hexaethyl- is known to react readily with a wide variety of organic compounds, making it useful for the preparation of complex molecules in organic chemistry. It also has potential applications in the field of material science, particularly for the development of advanced polymers and pharmaceuticals. Due to its versatility and reactivity, boranetriamine, N,N,N',N',N'',N''-hexaethyl- is a valuable compound with a range of potential uses in different industries.

Upstream product

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

Downstream Products

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

Relevant articles and documents

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.

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.