1,3,5-Tris(p-formylphenyl)benzene
| Catalog Number | Size | Price | Stock | Quantity |
|---|---|---|---|---|
| BPM-234467 | 2 g | $299 | In stock | |
| BPM-234467 | 5 g | $419 | In stock |
Product Information
Molecular Formula
C27H18O3
Molecular Weight
390.4
Description
1,3,5-Tris(p-formylphenyl)benzene is a pivotal compound extensively employed in the biomedical sector and assumes an indispensable function in synthesizing a myriad of pharmaceuticals, notably those aimed at combating ailments such as cancer and inflammation. By virtue of its distinctive configuration and characteristics, this compound assumes the role of an invaluable cornerstone for the advancement of ground-breaking pharmaceutical formulations.
Synonyms
5'-(4-Formylphenyl)-[1,1':3',1''-terphenyl]-4,4''-dicarbaldehyde; 4-[3,5-bis(4-formylphenyl)phenyl]benzaldehyde
IUPAC Name
4-[3,5-bis(4-formylphenyl)phenyl]benzaldehyde
SMILES
C1=CC(=CC=C1C=O)C2=CC(=CC(=C2)C3=CC=C(C=C3)C=O)C4=CC=C(C=C4)C=O
InChI
InChI=1S/C27H18O3/c28-16-19-1-7-22(8-2-19)25-13-26(23-9-3-20(17-29)4-10-23)15-27(14-25)24-11-5-21(18-30)6-12-24/h1-18H
InChI Key
ZCJZVMNBJKPQEV-UHFFFAOYSA-N
Boiling Point
612.3±55.0 °C(Predicted)
Melting Point
250 °C
Purity
95%
Density
Air Sensitive
Appearance
White to Light yellow to Light orange powder to crystal
Storage
Store under inert gas
Computed Properties
XLogP3
5.2
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
6
Exact Mass
390.125594432 g/mol
Monoisotopic Mass
390.125594432 g/mol
Topological Polar Surface Area
51.2Ų
Heavy Atom Count
30
Formal Charge
0
Complexity
470
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-114085388-A | Covalent organic framework material containing oxadiazole connecting element | 2021-12-23 |
| CN-113912805-A | Organic porous polymer for catalyzing cycloaddition of epoxide and carbon dioxide | 2021-11-14 |
| CN-113828169-A | polycoFs/bimetal MOFs composite membrane and preparation method thereof | 2021-10-20 |
| CN-113603912-A | Method for preparing high-crystallinity covalent organic framework film by using ionic liquid-water interface | 2021-07-17 |
| CN-113426158-A | Preparation method of quinolone drug pass-through solid-phase extraction column | 2021-06-26 |
| CN-113278122-A | Synthesis method of hydrogen bond induced high-stability porous covalent organogel material LNQZ-1 | 2021-06-26 |
| CN-113201148-A | Spiral infinite ordered growth COFs material and preparation method and application thereof | 2021-06-11 |
| CN-113388081-A | Double-chain polyethylene oxide modified covalent organic framework, preparation method and application thereof | 2021-05-31 |
| CN-113333021-A | Porous polymer supported palladium catalyst with high catalytic activity and application thereof in catalyzing Suzuki-Miyaura reaction | 2021-04-07 |
| CN-112973460-A | Crosslinked covalent organic framework desalting membrane and preparation method and application thereof | 2021-03-15 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 21666905 | 2011-08-21 | Selective gas sorption in a [2+3] 'propeller' cage crystal | Chemical communications (Cambridge, England) |
| 21721558 | 2011-08-03 | Crystalline covalent organic frameworks with hydrazone linkages | Journal of the American Chemical Society |
