181058-08-2

Basic information

• Product Name: 1,3,5-TRIS(BROMOMETHYL)-2,4,6-TRIETHYLBENZENE
• Synonyms: 1,3,5-TRIS(BROMOMETHYL)-2,4,6-TRIETHYLBENZENE;1,3,5-tri(broMoMethyl)-2,4,6-triethylbenzene;2,4,6-Triethyl-1,3,5-tris(bromomethyl)benzene;1,3,5-Tris(broMoMethyl)-2,4,6-triethylbenzene 98%
• CAS NO: 181058-08-2
• Molecular Formula: C₁₅H₂₁Br₃
• Molecular Weight: 441.04
• Product Categories: pharmacetical;Alkyl;Halogenated Hydrocarbons;Organic Building Blocks
• Mol File: 181058-08-2.mol
• Article Data: 38

Chemical Properties

• Melting Point: 172-177 °C
• Boiling Point: 392.3 °C at 760 mmHg
• Flash Point: 185.3 °C
• Appearance: /
• Density: 1.595 g/cm³
• Vapor Pressure: 5.21E-06mmHg at 25°C
• Refractive Index: 1.586
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• BRN: 7639256
• CAS DataBase Reference: 1,3,5-TRIS(BROMOMETHYL)-2,4,6-TRIETHYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-TRIS(BROMOMETHYL)-2,4,6-TRIETHYLBENZENE(181058-08-2)
• EPA Substance Registry System: 1,3,5-TRIS(BROMOMETHYL)-2,4,6-TRIETHYLBENZENE(181058-08-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 181058-08-2(Hazardous Substances Data)

Usage

General Description

1,3,5-TRIS(BROMOMETHYL)-2,4,6-TRIETHYLBENZENE is a chemical compound composed of three bromomethyl groups attached to a benzene ring, specifically at the 1,3,5 positions, and three ethyl groups attached at the 2,4,6 positions. 1,3,5-TRIS(BROMOMETHYL)-2,4,6-TRIETHYLBENZENE is commonly used as a crosslinking agent in polymer chemistry, as the bromomethyl groups can form covalent bonds with other molecules, creating a three-dimensional network. It is also used in the production of flame retardant materials and as a reagent in organic synthesis. The compound's properties and reactivity make it a valuable component in various industrial applications. However, it is important to handle this chemical with caution due to its potential toxic and hazardous nature.

InChI:InChI=1/C15H21Br3/c1-4-10-13(7-16)11(5-2)15(9-18)12(6-3)14(10)8-17/h4-9H2,1-3H3

Upstream product

• 71-43-2 benzene 
• 102-25-0 1,3,5-triethylbenzene 
• 123-63-7 paracetaldehyde 
• 50-00-0 formaldehyd 

Downstream Products

• 797818-01-0 1,3,5-tris-[(4,6-dimethyl-pyridin-2-yl)-aminomethyl]-2,4,6-triethylbenzene 
• 149525-65-5 1,3,5-triethyl-2,4,6-tris(aminomethyl)benzene 
• 954111-58-1 1,3,5-trimethylimidazole-2,4,6-triethyl benzene 
• 1095314-50-3 1,3,5-tris(4-nitrophenoxymethyl)-2,4,6-triethylbenzene 
• 661466-96-2 1,3,5-tris(2-nitrophenoxymethyl)-2,4,6-triethylbenzene 
• 1095517-58-0 hexaethyl 2,2',2''-(2,4,6-triethylbenzene-1,3,5-triyl)tris(methylene)trimalonate 
• 906565-55-7 2,4,6-triethylbenzene-1,3,5-tricarbaldehyde 
• 181058-09-3 1,3,5-tris(cyanomethyl)-2,4,6-triethylbenzene 
• 1260113-61-8 C₃₀H₄₈N₆O₃ 
• 1260113-63-0 C₃₀H₅₄N₆ 

Relevant articles and documents

Self-Assembly of Spherical Organic Molecules to Form Hollow Vesicular Structures in Water for Encapsulation of an Anticancer Drug and Its Release

Developing hierarchical supramolecular structures is important for better understanding of various biological functions and possibly generating new materials for biomedical applications. Herein, we report the first examples of functional vesicles derived from cationic spherical organic molecules (C1-C3) which were readily synthesized by reacting a C3-symmetric tris-benzimmidazole derivative (possessing a 1,3,5-ethyl substituted aromatic core) with 1,3,5-substituted tris-bromomethyl benzene derivatives. Vesicle formation by C1-C3 was probed by high-resolution microscopy (TEM and AFM), dynamic light scattering (DLS) and fluorescence microscopic imaging of calcein-loaded vesicles. One of the vesicles [Vesicle(C3)] displayed the ability to load the anticancer drug doxorubicin (DOX). The drug was subsequently released from DOX@Vesicle(C3) in a stimuli-responsive manner in presence of the well-known vesicle destroyer Triton X-100, as revealed by in vitro cell migration assay carried out on a highly aggressive human breast cancer cell line (MDA-MB-231).

From transient sulfenic acids toward peculiar sulfurated molecules

Sulfenic acids (R-SOH) frequently act as reactive intermediates in biological and synthetic chemistry. Among the numerous examples that Nature offers to our knowledge, cysteine-derived sulfenic acids are recognized as key intermediates in signal transduct

A Dichotomy in Cross-Coupling Site Selectivity in a Dihalogenated Heteroarene: Influence of Mononuclear Pd, Pd Clusters, and Pd Nanoparticles-The Case for Exploiting Pd Catalyst Speciation

Site-selective dihalogenated heteroarene cross-coupling with organometallic reagents usually occurs at the halogen proximal to the heteroatom, enabled by intrinsic relative electrophilicity, particularly in strongly polarized systems. An archetypical exam

Covalent organic cage compound material with acid stimulation response function and preparation method and application thereof

The invention belongs to the field of preparation of organic materials, and discloses synthesis and application of a covalent organic cage compound material with an acid stimulation response function. The preparation method is characterized by comprising

Photo-thermal platinum nanoparticle with mannose targeting as well as preparation method and application thereof

The invention discloses a photo-thermal platinum nanoparticle with mannose targeting as well as a preparation method and application thereof. The photo-thermal platinum nanoparticle with mannose targeting is formed by self-assembling a polymer carrier, tw