Tris(2-pyridylmethyl)amine

Product Information

Molecular Formula:
C18H18N4
Molecular Weight:
290.36
Description
ATRP for Everyone: Ligands and Initiators for the Clean Synthesis of Functional Polymers.
Synonyms
1-pyridin-2-yl-N,N-bis(pyridin-2-ylmethyl)methanamine
IUPAC Name
1-pyridin-2-yl-N,N-bis(pyridin-2-ylmethyl)methanamine
Canonical SMILES
C1=CC=NC(=C1)CN(CC2=CC=CC=N2)CC3=CC=CC=N3
InChI
InChI=1S/C18H18N4/c1-4-10-19-16(7-1)13-22(14-17-8-2-5-11-20-17)15-18-9-3-6-12-21-18/h1-12H,13-15H2
InChI Key
VGUWFGWZSVLROP-UHFFFAOYSA-N
Boiling Point
198 °C (lit.)
Melting Point
85-89 °C
Flash Point
219.2 °F
Purity
98%
Density
1.175 g/cm3
Appearance
Brown solid
Refractive Index
n20/D 1.455
LogP
3.07400

Safety Information

Hazards
H315 H319
Precautionary Statement
P264, P270, P301+P312, P330, and P501
Signal Word
Warning

Computed Properties

XLogP3
1.6
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
6
Exact Mass
290.153146591 g/mol
Monoisotopic Mass
290.153146591 g/mol
Topological Polar Surface Area
41.9Ų
Heavy Atom Count
22
Formal Charge
0
Complexity
262
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114057618-A Methionine optimized preparation method based on sulfuric acid indirect acidification method 2021-12-10
CN-114149351-A Methionine optimized preparation method based on sulfuric acid direct acidification method and sodium sulfate washing equipment 2021-12-10
CN-114044748-A Methionine optimized preparation method based on carbon dioxide acidification method 2021-12-09
CN-114163367-A Methionine environment-friendly preparation method based on carbon dioxide acidification method 2021-12-09
CN-113788909-A pH response type porous adsorption material and preparation method and application thereof 2021-09-07
CN-113736207-A Multi-component surface organic-inorganic composite nano particle and preparation method and application thereof 2021-08-17
CN-113083019-A Amphoteric substance-based polyamide nanofiltration membrane surface modification method 2021-03-29
CN-112574037-A Synthetic method of alpha, gamma-tetrachlorobutyrate 2021-02-20
CN-215856365-U System device for realizing stable output of nitric oxide 2021-02-08
CN-112755813-A Thin film composite membrane containing intermediate layer and preparation method and application thereof 2020-12-24

Literatures

PMID Publication Date Title Journal
23051175 2012-11-05 Kinetic and mechanistic aspects of atom transfer radical addition (ATRA) catalyzed by copper complexes with tris(2-pyridylmethyl)amine Inorganic chemistry
22905650 2012-09-03 Characterization of cobalt(III) hydroxamic acid complexes based on a tris(2-pyridylmethyl)amine scaffold: reactivity toward cysteine methyl ester Inorganic chemistry
22692585 2012-07-21 Improvement of durability of an organic photocatalyst in p-xylene oxygenation by addition of a Cu(II) complex Physical chemistry chemical physics : PCCP
22731779 2012-07-16 Capped-tetrahedrally coordinated Fe(II) and Co(II) complexes using a 'Click'-derived tripodal ligand: geometric and electronic structures Inorganic chemistry
22653336 2012-07-14 Synthesis, spectroscopic analysis and photolabilization of water-soluble ruthenium(III)-nitrosyl complexes Dalton transactions (Cambridge, England : 2003)
22458367 2012-04-16 Nonprecious metal catalysts for fuel cell applications: electrochemical dioxygen activation by a series of first row transition metal tris(2-pyridylmethyl)amine complexes Inorganic chemistry
22349513 2012-03-09 KLF10, transforming growth factor-β-inducible early gene 1, acts as a tumor suppressor Biochemical and biophysical research communications
22264120 2012-02-20 Evaluating the identity and diiron core transformations of a (μ-oxo)diiron(III) complex supported by electron-rich tris(pyridyl-2-methyl)amine ligands Inorganic chemistry
22246788 2012-02-13 100 picosecond diffraction catches structural transients of laser-pulse triggered switching in a spin-crossover crystal Chemistry (Weinheim an der Bergstrasse, Germany)
22277027 2012-02-08 Discrete complexes immobilized onto click-SBA-15 silica: controllable loadings and the impact of surface coverage on catalysis Journal of the American Chemical Society
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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