1,3,5-tris(Bromomethyl)benzene
Product Information
Molecular Formula
C9H9Br3
Molecular Weight
356.88
Description
1,3,5-tris(Bromomethyl)benzene is a bioactive compounds that is primarily harnessed for the synthesis of a pharmacopeia of compounds. It wields pivotal influence in pharmaceutical innovation, spawning new therapeutics specifically for the malignant cancer scourge and degenerative neural afflictions.
Synonyms
2,4,6-Tri(bromomethyl)benzene,Tribromomesitylene
IUPAC Name
1,3,5-tris(bromomethyl)benzene
SMILES
BrCc1cc(CBr)cc(CBr)c1
InChI
InChI=1S/C9H9Br3/c10-4-7-1-8(5-11)3-9(2-7)6-12/h1-3H,4-6H2
InChI Key
GHITVUOBZBZMND-UHFFFAOYSA-N
Boiling Point
352.2±37.0 °C(Predicted)
Melting Point
94-99 °C
Purity
97%
Density
2.005±0.06 g/cm3(Predicted)
Appearance
White to Almost white powder to crystal
Safety Information
Hazards
H314 H290
Precautionary Statement
P501 P260 P234 P264 P280 P390 P303 + P361 + P353 P301 + P330 + P331 P363 P304 + P340 + P310 P305 + P351 + P338 + P310 P406 P405
Signal Word
Danger
Computed Properties
XLogP3
3.6
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
3
Exact Mass
355.82339 g/mol
Monoisotopic Mass
353.82544 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
91.2
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-113999372-A | Phosphorus-containing super-crosslinked porous organic polymer material and preparation method and application thereof | 2021-12-21 |
| CN-114031786-A | Preparation method and application of metal organic framework for alkane C-H bond activation coupling reaction | 2021-11-06 |
| CN-113996273-A | Polyion liquid adsorption film, preparation method thereof and application thereof in rhenium adsorption | 2021-11-04 |
| CN-113764725-A | Solid electrolyte capable of in-situ polymerization and all-solid-state battery comprising same | 2021-08-31 |
| CN-113233989-A | 1, 4-trihydroxyethylbenzdiammonium sulfate, 1,3, 5-trihydroxyethylbenztriammonium sulfate, synthesis and application thereof | 2021-05-27 |
| CN-113292724-A | Preparation method of pyridine-rich cationic covalent triazine polymer | 2021-05-17 |
| CN-112941655-A | Nano-fiber bilirubin adsorbent and preparation method thereof | 2021-03-30 |
| CN-113144816-A | Metal complex ion functionalized polyion liquid and preparation method and application thereof | 2021-03-12 |
| CN-112960656-A | Preparation method of vanadium nitride nanoparticle composite material for lithium-sulfur battery | 2021-02-02 |
| CN-112574065-A | Preparation method of (benzene-1, 3, 5-triacyl) acetonitrile | 2020-12-30 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 21837224 | 2011-07-01 | 1,1'-[(5-Hy-droxy-methyl-1,3-phenyl-ene)bis-(methyl-ene)]dipyridin-4(1H)-one monohydrate | Acta crystallographica. Section E, Structure reports online |
| 21633159 | 2011-06-01 | 1,3,5-Tris(bromomethyl)benzene | Acta crystallographica. Section C, Crystal structure communications |
| 15453773 | 2004-10-06 | A highly efficient, preorganized macrobicyclic receptor for halides based on CH... and NH...anion interactions | Journal of the American Chemical Society |
| 14986965 | 2004-03-04 | Synthesis of a macrobicycle incorporating the tris(pyrazolyl)methane ligand | Organic letters |
