1,3,5-Tris(4-aminophenyl)benzene
Product Information
Molecular Formula
C24H21N3
Molecular Weight
351.45
Description
1,3,5-Tris(4-aminophenyl)benzene (CAS# 118727-34-7) is a useful reagent for catalytic asymmetric synthesis of chiral covalent compounds.
Synonyms
4-[3,5-bis(4-aminophenyl)phenyl]aniline; 4-[3,5-bis(4-aminophenyl)phenyl]aniline
IUPAC Name
4-[3,5-bis(4-aminophenyl)phenyl]aniline
SMILES
C1=CC(=CC=C1C2=CC(=CC(=C2)C3=CC=C(C=C3)N)C4=CC=C(C=C4)N)N
InChI
InChI=1S/C24H21N3/c25-22-7-1-16(2-8-22)19-13-20(17-3-9-23(26)10-4-17)15-21(14-19)18-5-11-24(27)12-6-18/h1-15H,25-27H2
InChI Key
QHQSCKLPDVSEBJ-UHFFFAOYSA-N
Boiling Point
576.3±45.0 °C (Predicted)
Melting Point
165 °C
Purity
> 93.0 % (T) (HPLC)
Density
Air Sensitive
Appearance
White to brown powder to crystal
Storage
Store under inert gas
LogP
7.17780
Safety Information
Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word
Warning
Computed Properties
XLogP3
3.9
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
3
Exact Mass
351.173547683 g/mol
Monoisotopic Mass
351.173547683 g/mol
Topological Polar Surface Area
78.1Ų
Heavy Atom Count
27
Formal Charge
0
Complexity
364
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-113980338-A | Thermoplastic polyurethane foaming particles, preparation method and application thereof in low-temperature bending resistant sole material | 2021-12-09 |
| CN-114106276-A | Preparation method of shape-controllable covalent organic framework material | 2021-12-07 |
| CN-114146572-A | Preparation method of amide chain segment embedded covalent organic framework composite membrane and filter membrane thereof | 2021-12-07 |
| CN-114130414-A | Preparation method of graphite type carbon nitride material, active catalyst and application | 2021-12-06 |
| CN-114028565-A | 3D-COF drug-loading system for treating breast cancer and preparation method thereof | 2021-11-30 |
| CN-113929923-A | Nano spherical covalent organic framework and preparation method and application thereof with controllable particle size | 2021-11-29 |
| CN-114015238-A | Insulation heat conduction gasket containing COF (chip on film) coated carbon fibers and preparation method thereof | 2021-11-26 |
| CN-114047341-A | Biological probe and biological immunosensor for detecting bungarus venosus and method for detecting bungarus venosus based on proportional signal | 2021-11-18 |
| CN-114177888-A | Preparation of GO/COFs composite material and application of GO/COFs composite material in organic pollutant adsorption | 2021-11-15 |
| CN-114015066-A | Covalent organic framework materials, methods of making and uses thereof | 2021-11-12 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 17912412 | 2007-10-21 | Control of ionic conductivity of ionic liquid/photoresponsive poly(amide acid) gels by photoirradiation | Chemical communications (Cambridge, England) |
| 17705307 | 2007-01-01 | Multicomponent dynamic covalent assembly of a rhombicuboctahedral nanocapsule | Chemistry (Weinheim an der Bergstrasse, Germany) |
| 17037872 | 2006-08-01 | Triphenyl benzene-bridged fluorescent silsesquioxane: shape-controlled hybrid silicas by hydrolytic conditions | Journal of nanoscience and nanotechnology |
| 16470770 | 2006-04-12 | Helical stacking tuned by alkoxy side chains in pi-conjugated triphenylbenzene discotic derivatives | Chemistry (Weinheim an der Bergstrasse, Germany) |
