116412-90-9

Basic information

• Product Name: 3,4-DIMETHOXY-4'-BROMOBENZOPHENONE
• Synonyms: 3,4-DIMETHOXY-4'-BROMOBENZOPHENONE;3,4-DIMETHOXY-4''-BROMOBENZOPHENONE 99.0%;4-Bromo-3',4'-dimethoxybenzophenone
• CAS NO: 116412-90-9
• Molecular Formula: C₁₅H₁₃BrO₃
• Molecular Weight: 321.16592
• Product Categories: Naphthyridine,Quinoline
• Mol File: 116412-90-9.mol

Chemical Properties

• Melting Point: 116-119 °C
• Boiling Point: 426.6±40.0 °C(Predicted)
• Appearance: /
• Density: 1.385±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3,4-DIMETHOXY-4'-BROMOBENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIMETHOXY-4'-BROMOBENZOPHENONE(116412-90-9)
• EPA Substance Registry System: 3,4-DIMETHOXY-4'-BROMOBENZOPHENONE(116412-90-9)

Safety Data

• Hazardous Substances Data: 116412-90-9(Hazardous Substances Data)

Usage

Uses

Used in Perfumery and Cosmetics Industry:
3,4-Dimethoxy-4'-bromobenzophenone is used as a UV stabilizer and absorber for protecting perfumes and cosmetics from UV degradation, ensuring their longevity and effectiveness.
Used in Pharmaceutical Products:
3,4-Dimethoxy-4'-bromobenzophenone is used as an intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Plastics Industry:
3,4-Dimethoxy-4'-bromobenzophenone is used as a UV stabilizer in plastics to prevent UV-induced degradation, enhancing the durability and performance of plastic materials.
Used in Chemical Synthesis and Laboratory Research:
Due to the presence of the bromine atom, 3,4-dimethoxy-4'-bromobenzophenone is more commonly used in chemical synthesis and laboratory research for the development of new compounds and materials with specific properties and applications.

Upstream product

• 586-75-4 4-chlorobenzoyl chloride 
• 91-16-7 1,2-dimethoxybenzene 
• 586-76-5 4-Bromobenzoic acid 

Downstream Products

• 886493-86-3 (4-bromophenyl)( 4,5-dimethoxy-2-nitrophenyl)-methanone 
• 1016509-04-8 (3,4-dimethoxyphenyl)(4-bromophenyl)methylamine 
• 1496524-39-0 isopropyl((2S)-1-(((3,4-dimethoxylphenyl)(4-bromophenyl)methyl)amino)-3-methyl-1-oxobutan-2-yl)carbamate 
• 1620077-23-7 (3,4-dimethoxyphenyl)(4-bromophenyl)methanone oxime 
• 116413-44-6 C₂₀H₂₃NO₃ 

Relevant articles and documents

P -Selective (sp2)-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis

p-Selective (sp2)-C-H functionalization of electron rich arenes has been achieved for acylation and alkylation reactions, respectively, with acyl/alkylselenides by organic photoredox catalysis involving an interesting mechanistic pathway.

Design, synthesis, and fungicidal activity of novel carboxylic acid amides represented by N-benzhydryl valinamode carbamates

Carboxylic acid amide (CAA) fungicides are an important class of agricultural fungicide with oomycete activity and low toxicity toward mammalian cells. To find CAA analogues with high activity against resistant pathogens, a series of substituted N-benzhydryl valinamide carbamate derivatives were designed and synthesized by introducing substituted aromatic rings into valinamide carbamate leads. Bioassays showed that some title compounds exhibited very good in vitro fungicidal activity against Phytophthora capsici and in vivo fungicidal activities against Pseudoperonospora cubensis. Topomer CoMFA was performed to explore the structure-activity relationship on the basis of the in vitro data. The dimethoxy substituted aromatic analogue 9e was found to display higher in vitro fungicidal activity against Phytophthora capsici than iprovalicarb but lower activity than mandipropamid, and higher in vivo fungicidal activity against Pseudoperonospora cubensis than dimethomorph at a dosage of 6.25 μg mL-1. This journal is the Partner Organisations 2014.