593231-72-2

Basic information

• Product Name: 1,3-Benzenediol, 2-bromo-5-ethenyl- (9CI)
• Synonyms: 1,3-Benzenediol, 2-bromo-5-ethenyl- (9CI)
• CAS NO: 593231-72-2
• Molecular Formula: C8H7BrO2
• Molecular Weight: 215.04398
• Product Categories: ALCOHOL
• Mol File: 593231-72-2.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-Benzenediol, 2-bromo-5-ethenyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzenediol, 2-bromo-5-ethenyl- (9CI)(593231-72-2)
• EPA Substance Registry System: 1,3-Benzenediol, 2-bromo-5-ethenyl- (9CI)(593231-72-2)

Safety Data

• Hazardous Substances Data: 593231-72-2(Hazardous Substances Data)

Usage

Structure

A derivative of vanillyl alcohol with a bromine atom and an ethenyl group

Usage

a. Precursor in the synthesis of various organic compounds
b. Used in the production of pharmaceuticals and fragrances
c. Potential use as a flavoring agent in food products
d. Potential applications in medicinal chemistry due to structural similarity to natural phenolic compounds

Limitations

a. Limited direct uses due to potential health and environmental risks
b. May require further processing or modification for specific applications

Upstream product

• 124112-23-8 {B(C₆H₄-4-CHBrCH₃)O}3 
• 7459-73-6 (4-Vinylphenyl)magnesium chloride 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 688-74-4 boric acid tributyl ester 
• 7439-95-4 magnesium 
• 1073-67-2 4-vinylbenzyl chloride 
• 121-43-7 Trimethyl borate 
• 42728-38-1 (4-(1,2-dibromoethyl)phenyl)boronic acid 
• 91113-71-2 tris(4-ethyl phenyl) boroxine 

Downstream Products

• 142013-51-2 O,O'-(4-vinyl-phenylboranediyl)-L_g-tartaric acid diethyl ester 
• 14559-99-0 diethoxy-(4-vinyl-phenyl)-borane 
• 55032-29-6 (R)-2-(4-vinyl-phenyl)-[1,3,2]dioxaborolane-4-carboxylic acid methyl ester 
• 55032-32-1 (R)-2-(4-vinyl-phenyl)-[1,3,2]dioxaborolane-4-carboxylic acid 4-nitro-benzyl ester 
• 1394291-71-4 C₁₈H₁₉N₃O 
• 1394291-70-3 C₃₆H₃₅N₇O₂ 
• 3139-85-3 4-vinylbenzophenone 
• 20912-50-9 4-benzoylbenzaldehyde 
• 227778-64-5 N-benzyloxycarbonyl-4-vinylaniline 

Relevant articles and documents

Superacidic porous polymer catalyst and its application in esterification of carboxylic acid

Two solid acid catalysts, SAC1 and SAC2, with porous structure obtained from mesoporous hard template were synthesized and characterized by Fourier transform infrared spectroscopy, acid-base titration, nitrogen adsorption/desorption, scanning electron mic

Room-temperature self-healing polymers based on dynamic-covalent boronic esters

Cross-linked polymers constructed with dynamic-covalent boronic esters were synthesized via photoinitiated radical thiol-ene click chemistry. Because the reversibility of the boronic ester cross-links was readily accessible, the resulting materials were capable of undergoing bond exchange to covalently mend after failure. The reversible bonds of the boronic esters were shown to shift their exchange equilibrium at room temperature when exposed to water. Nevertheless, the materials were observed to be stable and hydrophobic and absorbed only minor amounts of water over extended periods of time when submerged in water or exposed to humid environments. The facile reversibility of the networks allowed intrinsic self-healing under ambient conditions. Highly efficient self-healing of these bulk materials was confirmed by mechanical testing, even after subjecting a single site to multiple cut-repair cycles. Several variables were considered for their effect on materials properties and healing, including cross-link density, humidity, and healing time.

Gels and multilayer surface structures from boronic acid containing polymers

Boronic acid containing polymers are used to form bioinert gels and multilayer surface structures. These polymers form crosslinked hydrogels, which are highly swollen in water. The crosslinking can either be chemical or physical. Water soluble polymers containing boronic acid groups, such as phenylboronic acid (PBA), can be physically crosslinked by mixing the polymers in water with other polymers containing hydroxyls or carboxylic acids. Alternatively, surfaces can be treated by stepwise incubation with a solution of the boronic acid containing polymer, followed by incubation with a solution of a diol or carboxylic acid containing polymer. Many successive layers can be generated, increasing the thickness of the formed structure at each step. The bioinert gel or surface coating can be used for passivating the surfaces of medical implants (especially those based on transplanted tissue), or for passivating the surfaces of tissues in situ, decreasing the incidence or severity of such pathologic conditions as the formation of post-surgical adhesions, and thrombosis following angioplasty.