608-72-0

Basic information

• Product Name: 1,3,5-TribroMo-2,4,6-TriMethyl-Benzene
• Synonyms: 1,3,5-Tribromotrimethylbenzene;1,3,5-Trisbromomesitylene;ar-Tribromomesitylene;NSC 97124;Benzene,1,3,5-tribromo-2,4,6-trimethyl-;2,4,6-Tribromo-1,3,5-trimethylbenzene;1,3,5-TribroMo-2,4,6-TriMethyl-Benzene;2,4,6-Tribromo-2,4,6-trimethyl-benzene
• CAS NO: 608-72-0
• Molecular Formula: C₉H₉Br₃
• Molecular Weight: 356.87976
• EINECS: -0
• Mol File: 608-72-0.mol
• Article Data: 22

Chemical Properties

• Melting Point: 225.5-226.5℃
• Boiling Point: 329.3°C at 760 mmHg
• Flash Point: 149.5°C
• Appearance: /
• Density: 1.91g/cm³
• Vapor Pressure: 0.000342mmHg at 25°C
• Refractive Index: 1.598
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform (Heated), Hexanes (Slightly, Heated)
• CAS DataBase Reference: 1,3,5-TribroMo-2,4,6-TriMethyl-Benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-TribroMo-2,4,6-TriMethyl-Benzene(608-72-0)
• EPA Substance Registry System: 1,3,5-TribroMo-2,4,6-TriMethyl-Benzene(608-72-0)

Safety Data

• Hazardous Substances Data: 608-72-0(Hazardous Substances Data)

Usage

Uses

1,3,5-Tribromo-2,4,6-Trimethylbenzene is a useful reagent for preparing highly durable superhydrophobic nanothorn arrays.

InChI:InChI=1/C9H9Br3/c1-4-7(10)5(2)9(12)6(3)8(4)11/h1-3H3

Upstream product

• 108-67-8 1,3,5-trimethyl-benzene 
• 7726-95-6 bromine 
• 7697-37-2 nitric acid 
• 13151-55-8 ethylcycloheptane 
• 4516-10-3 1-cyclohexyl-2,4,6-trimethylbenzene 
• 7727-15-3 aluminium bromide 
• 7439-89-6 iron 
• 75-15-0 carbon disulfide 
• 7446-70-0 aluminium trichloride 
• 576-83-0 2,4,6-trimethylphenyl bromide 
• 52629-46-6 (2,4,6-trimethyl-phenyl)acetyl chloride 
• 3453-83-6 mesitylene sulfonic acid 
• 7732-18-5 water 
• 7664-93-9 sulfuric acid 

Downstream Products

• 1206-85-5 2,4,6-trimethylbenzene-1,3,5-tricarbonitrile 
• 128014-48-2 3,5-Dibromo-2,4,6-trimethylbenzaldehyde 
• 643027-92-3 1,3,5-tris[(E)-2-(4-cyanophenyl)ethenyl]-2,4,6-trimethylbenzene 
• 643027-87-6 1,3,5-trimethyl-2,4,6-tris[(E)-2-(4-propoxyphenyl)ethenyl]benzene 
• 643027-89-8 1,3,5-tris[(E)-2-(4-hexyloxyphenyl)ethenyl]-2,4,6-trimethylbenzene 
• 643027-90-1 1,3,5-tris[(E)-2-(4-decyloxyphenyl)ethenyl]-2,4,6-trimethylbenzene 
• 191529-08-5 1,3,5-tribromo-2,4,6-tris(hydroxymethyl)benzene 
• 103158-54-9 1,3,5-tris-benzenesulfonyl-2,4,6-trimethyl-benzene 
• 1402134-31-9 1,3,5-tribromo-2,4,6-tri(hydroxyiminomethyl)benzene 
• 60510-14-7 1,3,5-tribromo-2,4,6-tricyanobenzene 
• 2195343-70-3 1,3,5-trimethyl-2,4,6-tris(4-formylphenyl)benzene 
• 643027-94-5 1,3,5-tris[(E)-2-(4-decyloxyphenyl)ethenyl]-2,4,6-tris[(diethoxyphosphoryl)methyl]benzene 
• 643027-93-4 1,3,5-tris[(diethoxyphosphoryl)methyl]-2,4,6-tris[(E)-2-(4-hexyloxyphenyl)ethenyl]benzene 
• 643027-88-7 1,3,5-tris[(diethoxyphosphoryl)methyl]-2,4,6-tris[(E)-2-(4-propoxyphenyl)ethenyl]benzene 

Relevant articles and documents

Collective In-Plane Molecular Rotator Based on Dibromoiodomesitylene π-Stacks

Interest in artificial solid-state molecular rotator systems is growing as they enable systems to be designed for achieving specific physical functions. The phase transition behavior of four halomesitylene crystals indicated dynamic in-plane molecular rot

2D-Covalent Organic Frameworks with Interlayer Hydrogen Bonding Oriented through Designed Nonplanarity

We report the synthesis and characterization of a new class of 2D-covalent organic frameworks, called COFamides, whose layers are held together by amide hydrogen bonds. To accomplish this, we have designed monomers with a nonplanar structure that arises f

Octupolar organometallic Pt(II) NCN-pincer complexes; Synthesis, electronic, photophysical, and NLO properties

A series of organometallic octupolar 1,3,5-substituted-2,4,6-styryl-benzene complexes was synthesized by post-modification of parent [PtCl(NCN-CHO-4)], i.e. 1,3,5-tri-R-2,4,6-tris[(4-(PtCl)(3,5-bis[(dimethylamino)methyl]styryl)]benzene (NCN = [C6H2(CH2NMe2)2-2,6]– in which R = OMe, H, Br (1–3). Their synthesis involved a triple Horner-Wadsworth-Emmons reaction of [PtCl(NCN-CHO-4)] with the appropriate tris[(diethoxyphosphoryl)]methyl]benzene derivative. The 195Pt{1H} NMR chemical shift reflects the electronic properties of the π-system to which it is connected. The UV/Vis bands of the octupolar platinum complexes are only slightly red-shifted (by 5–12 nm) with respect to those of corresponding stilbenoid Pt-Cl pincer compounds (i.e., the separate branches), suggesting that there is only a limited electronic interaction between these branches. The fluorescence Stokes shift, quantum yields and lifetimes of 1–3 also are of the same order of magnitude as those of stilbenoid Pt-Cl pincer compounds, indicating that a dipolar excited state is formed, which is localized on one of the three branches. The hyper-Rayleigh scattering technique revealed hyperpolarizabilites βHRS of 430, 870 and 183 × 10?30 esu for 1, 2 and 3, respectively, which are among the highest for transition metal complexes. The highest value was found for the compound lacking a donor or acceptor group at the central core, lending support to the idea that dispersion overwhelms charge transfer in determining the magnitude of the first hyperpolarizability in octupolar compounds.