2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde
| Catalog Number | Size | Price | Stock | Quantity |
|---|---|---|---|---|
| BPM-366280 | 5 g | $299 | In stock |
Product Information
Molecular Formula
C9H6O6
Molecular Weight
210.14
Description
2,4,6-Trihydroxybenzaldehyde-1,3,5-trisodium sulfonate is a key compound in biomedicine, employed primarily as an intermediate in drug synthesis. It has antioxidant properties that aid in the study of diseases caused by oxidative stress, such as cancer, inflammation, and cardiovascular disease.
Synonyms
2,4,6-triformylphloroglucinol; triformylphloroglucinol
IUPAC Name
2,4,6-trihydroxybenzene-1,3,5-tricarbaldehyde
SMILES
C(=O)C1=C(C(=C(C(=C1O)C=O)O)C=O)O
InChI
InChI=1S/C9H6O6/c10-1-4-7(13)5(2-11)9(15)6(3-12)8(4)14/h1-3,13-15H
InChI Key
KAPNIDMXEKQLMQ-UHFFFAOYSA-N
Boiling Point
233.8±40.0 °C at 760 mmHg
Melting Point
199-200 °C
Purity
>98.0%(GC)
Density
1.755±0.06 g/cm3
Appearance
White to Light yellow to Light red powder to crystal
Storage
<0°C
Safety Information
Hazards
H315 H319
Precautionary Statement
P264 P280 P302 + P352 P337 + P313 P305 + P351 + P338 P362+P364 P332 + P313
Computed Properties
XLogP3
0.9
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
6
Rotatable Bond Count
3
Exact Mass
210.01643791 g/mol
Monoisotopic Mass
210.01643791 g/mol
Topological Polar Surface Area
112Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
205
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-114188669-A | Functional diaphragm and preparation method and application thereof | 2021-12-21 |
| CN-113461933-A | Polymer self-supporting nano film, continuous and macro preparation method and application thereof | 2021-06-01 |
| CN-113461887-A | One-dimensional nanochannel self-supporting covalent organic framework membrane for salt difference power generation and application thereof | 2021-01-28 |
| CN-112808006-A | High-rejection-rate covalent organic framework membrane, and raw material composition and preparation method thereof | 2021-01-08 |
| WO-2022038627-A1 | Three dimensional cof-graphene and cof-cnt hybrids with remarkable chemical stability for methane storage | 2020-08-17 |
| CN-111689918-A | Functional diaphragm coating material for protecting lithium metal negative electrode and preparation method and application thereof | 2020-04-30 |
| CN-111689918-B | Functional diaphragm coating material for protecting lithium metal negative electrode and preparation method and application thereof | 2020-04-30 |
| WO-2021220166-A1 | Electrode separators | 2020-04-28 |
| WO-2021203464-A1 | Pigment particle template, manufacturing method therefor and preparation method for pigment dispersion liquid | 2020-04-08 |
| WO-2021198868-A1 | Method of tuning the electronic energy level of covalent organic framework for crafting high-rate na-ion battery anode | 2020-03-28 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 22730217 | 2012-07-23 | Octupolar merocyanine dyes: a new class of nonlinear optical chromophores | Chemistry (Weinheim an der Bergstrasse, Germany) |
| 21052602 | 2010-12-28 | Synthesis and characterization of a trinuclear Cu(II)3 complex bridged by an extended phloroglucinol-ligand: implications for a rational enhancement of ferromagnetic interactions | Dalton transactions (Cambridge, England : 2003) |
| 14535719 | 2003-10-16 | Highly stable keto-enamine salicylideneanilines | Organic letters |