76693-57-7

Basic information

• Product Name: 4-BROMO-4'-METHYLBENZOPHENONE
• Synonyms: 4-BROMO-4'-METHYLBENZOPHENONE;AKOS AKM01175;OTAVA-BB 1043941;UKRORGSYN-BB BBV-5118799
• CAS NO: 76693-57-7
• Molecular Formula: C₁₄H₁₁BrO
• Molecular Weight: 275.14
• Mol File: 76693-57-7.mol
• Article Data: 34

Chemical Properties

• Boiling Point: 377.6°C at 760 mmHg
• Flash Point: 80.6°C
• Appearance: /
• Density: 1.375g/cm³
• Vapor Pressure: 6.67E-06mmHg at 25°C
• Refractive Index: 1.601
• CAS DataBase Reference: 4-BROMO-4'-METHYLBENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-4'-METHYLBENZOPHENONE(76693-57-7)
• EPA Substance Registry System: 4-BROMO-4'-METHYLBENZOPHENONE(76693-57-7)

Safety Data

• Hazardous Substances Data: 76693-57-7(Hazardous Substances Data)

Usage

Description

4-BROMO-4'-METHYLBENZOPHENONE is a benzophenone derivative featuring a bromine substituent at the 4-position and a methyl group at the 4'-position. It is a chemical compound that finds applications in various industries, including pharmaceuticals, cosmetics, and textiles.

Uses

Used in Photopolymerization:
4-BROMO-4'-METHYLBENZOPHENONE is used as a photoinitiator in photopolymerization reactions for its ability to initiate the curing process of resins and coatings upon exposure to light.
Used in Organic Synthesis:
4-BROMO-4'-METHYLBENZOPHENONE is utilized in the synthesis of other organic compounds, serving as a key intermediate in chemical reactions.
Used in UV-Curable Materials Production:
4-BROMO-4'-METHYLBENZOPHENONE is used as a building block in the production of UV-curable materials, contributing to the development of innovative products in various applications.
Used in Pharmaceutical Research:
4-BROMO-4'-METHYLBENZOPHENONE exhibits potential biological activity and is being researched for its potential applications as an anti-tumor agent, indicating its importance in the field of medicinal chemistry.
Used in Cosmetics Industry:
In the cosmetics industry, 4-BROMO-4'-METHYLBENZOPHENONE may be used for its properties that can enhance the performance of certain cosmetic products, although specific applications are not detailed in the provided materials.
Used in Textile Industry:
4-BROMO-4'-METHYLBENZOPHENONE is also used in the textile industry, potentially for its role in the development of UV-curable materials that can be applied to textiles for various functional or aesthetic purposes.
It is important to handle 4-BROMO-4'-METHYLBENZOPHENONE with care due to its potential health hazards and environmental impact, ensuring proper safety measures are in place during its use and disposal.

InChI:InChI=1/C14H11BrO/c1-10-2-4-11(5-3-10)14(16)12-6-8-13(15)9-7-12/h2-9H,1H3

Upstream product

• 586-76-5 4-Bromobenzoic acid 
• 108-88-3 toluene 
• 586-75-4 4-chlorobenzoyl chloride 
• 29334-17-6 (4-bromophenyl)(4-methylphenyl)methanol 
• 108-86-1 bromobenzene 
• 79-37-8 oxalyl dichloride 
• 34176-08-4 sodium 4-bromobenzenesulfinate 
• 104-85-8 para-methylbenzonitrile 
• 36228-65-6 2-pyridyl 4-methylbenzoate 
• 5467-74-3 4-Bromophenylboronic acid 
• 99-94-5 p-Toluic acid 
• 17100-53-7 1-bromo-4-(4-methylbenzyl)benzene 
• 67-66-3 chloroform 
• 624-31-7 4-tolyl iodide 

Downstream Products

• 51310-30-6 4-(4'-bromobenzoyl)benzoic acid 
• 685887-85-8 methyl 11-[4-(4-methylbenzoyl)-phenyl]-undecanoate 
• 685887-86-9 acetic acid 11-[4-(4-methyl-benzoyl)-phenyl]-undecyl ester 
• 82745-40-2 4-(4-sulfamoyl-1,1'-biphenyl-4'-carbonyl)benzoic acid 
• 685887-87-0 11-[4-(4-methyl-benzoyl)-phenyl]-undecanoic acid anhydride 
• 685888-15-7 11-[4-(4-methylbenzoyl)phenyl]-undec-5-enoic acid anhydride 
• 685888-03-3 1-O-{11-[4-(4-methylbenzoyl)-phenyl]-undecyl}-2-O-(4-methoxybenzyl)-sn-glycero-3-phosphocholine 
• 685887-95-0 1-O-{11-[4-(4-methylbenzoyl)-phenyl]-undecyl}-2-O-triisopropylsilyl-3-O-tosyl-sn-glycerol 
• 685888-00-0 1-O-{11-[4-(4-methylbenzoyl)-phenyl]-undecyl}-2-O-(4-methoxybenzyl)-3-O-tosyl-sn-glycerol 
• 685888-12-4 1-O-{11-[4-(4-methylbenzoyl)phenyl]-5-undecenyl}-2-O-(4-methoxybenzyl)-sn-glycero-3-phosphocholine 
• 685887-98-3 1-O-{11-[4-(4-methylbenzoyl)-phenyl]-undecyl}-2-O-tetrahydropyranyl-3-O-tosyl-sn-glycerol 
• 685888-09-9 1-O-{11-[4-(4-methylbenzoyl)phenyl]-5-undecenyl}-2-O-(4-methoxy)benzyl-3-O-tosyl-sn-glycerol 

Relevant articles and documents

A dialdehyde-diboronate-functionalized AIE luminogen: Design, synthesis and application in the detection of hydrogen peroxide

A dialdehyde-diboronate-functionalized tetraphenylethene (TPE-DABF) was reported as a H2O2-specific AIE luminogen. TPE-DABF, bearing multiple reductive units (aldehyde, boronate and fructose) in one molecule, afforded an excellent H

Selective oxidation of alkenes to carbonyls under mild conditions

Herein, a practical and sustainable method for the synthesis of aldehydes, ketones, and carboxylic acids from an inexpensive olefinic feedstock is described. This transformation features very sustainable and mild conditions and utilizes commercially available and inexpensive tetrahydrofuran as the additive, molecular oxygen as the sole oxidant and water as the solvent. A wide range of substituted alkenes were found to be compatible, providing the corresponding carbonyl compounds in moderate-to-good yields. The control experiments demonstrated that a radical mechanism is responsible for the oxidation reaction.

Aryl aldiketone and synthesis method thereof

The invention discloses an aryl aldehyde ketone and a synthesis method thereof, wherein an aryl aldehyde is synthesized from cheap olefin as a raw material. A commercially available inexpensive olefin is used as a raw material, ether is used as an additive, molecular oxygen serves as a sole oxidizing agent, water is used as a solvent, and the aldehyde and ketone are synthesized by column chromatography under a photocatalytic condition. The invention has the advantages of mild reaction conditions, green and environmental protection, simple experimental operation, good reaction selectivity, high product yield and the like.