29162-91-2

Basic information

• Product Name: 1,3,2-Diazaborine, 2-bromohexahydro-1,3-dimethyl-
• CAS NO: 29162-91-2
• Molecular Formula: C5H12BBrN2
• Molecular Weight: 190.879
• Mol File: 29162-91-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3,2-Diazaborine, 2-bromohexahydro-1,3-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,2-Diazaborine, 2-bromohexahydro-1,3-dimethyl-(29162-91-2)
• EPA Substance Registry System: 1,3,2-Diazaborine, 2-bromohexahydro-1,3-dimethyl-(29162-91-2)

Safety Data

• Hazardous Substances Data: 29162-91-2(Hazardous Substances Data)

Usage

Type of compound

Boron-containing heterocyclic compound

Potential applications

a. Organic chemistry
b. Medicinal chemistry
c. Pharmaceutical agent
d. Synthesis of complex organic compounds

Structure

Unique structure that contributes to its potential applications

Research status

Further research needed to fully understand potential applications and properties

Upstream product

• 121-44-8 triethylamine 
• 111-33-1 1,3-bis(methylamino)propane 

Relevant articles and documents

Boron-nitrogen compounds. XXXIV. Preparation and some properties of 2-halo-1,3,2-diazaboracycloalkanes

A series of 2-halo-1,3,2-diazaboracycloalkanes has been prepared by (a) the interaction of trialkylamine-trihaloboranes with alphatic α,ω-diamines, (b) displacement of dimethylamino groups of 2-dimethylamino-1,3,2-diazaboracycloalkanes with halogen through interaction with boron trihalides, and (c) a transhalogenation reaction. The 2-halo-1,3,2-diazaboracycloalkanes are thermally rather stable but are very reactive toward moisture and oxygen. The boron-bonded halogen is readily replaced by organic groups through interaction with Grignard reagents. All compounds have a characteristic BN absorption in the 1510-1540-cm-1 region of their infrared spectra and the proton magnetic resonance spectra are consistent with their structure. In the mass spectra, the parent peaks P+ are generally less abundant than the (P - 1)+ peaks.