Tris(2-benzimidazolylmethyl)amine

Catalog Number	ACM64019574-3
CAS	64019-57-4
Structure
Description	Tris(2-benzimidazolylmethyl)amine, commonly referred to as TBM, is a heterocyclic amine that is widely used in scientific research. It is a versatile compound that can be used in a variety of applications, including synthesis, scientific research, and lab experiments. TBM has a number of biochemical and physiological effects and is known to have a wide range of applications.
IUPAC Name	1-(1H-benzimidazol-2-yl)-N,N-bis(1H-benzimidazol-2-ylmethyl)methanamine
Molecular Weight	407.5 g/mol
Molecular Formula	C24H21N7
Canonical SMILES	C1=CC=C2C(=C1)NC(=N2)CN(CC3=NC4=CC=CC=C4N3)CC5=NC6=CC=CC=C6N5
InChI	InChI=1S/C24H21N7/c1-2-8-17-16(7-1)25-22(26-17)13-31(14-23-27-18-9-3-4-10-19(18)28-23)15-24-29-20-11-5-6-12-21(20)30-24/h1-12H,13-15H2,(H,25,26)(H,27,28)(H,29,30)
InChI Key	YQIGEJHOYBUSLR-UHFFFAOYSA-N
Application	TBM has a number of scientific research applications. It has been used as a model compound for studying the structure and reactivity of heterocyclic compounds. It has also been used as a reagent for synthesizing other heterocyclic compounds, as well as for studying the reactivity of other molecules. Additionally, TBM has been used in a variety of biological studies, including studies of enzyme inhibition, protein-protein interactions, and drug-receptor interactions.
GHS Pictogram	Irritant
Properties	TBM has a number of biochemical and physiological effects. It has been shown to inhibit the activity of certain enzymes, such as cyclooxygenase and lipoxygenase. It has also been shown to interact with certain proteins, such as G protein-coupled receptors. Additionally, TBM has been shown to have anti-inflammatory, anti-oxidant, and anti-cancer properties.