4073-35-2

Basic information

• Product Name: 3,5-DIBROMO-4-METHOXYBENZOIC ACID
• Synonyms: RARECHEM AL BO 0304;3,5-DIBROMO ANISIC ACID;3,5-DIBROMO-4-METHOXYBENZOIC ACID;3,5-DIBROMO-4-ANISIC ACID
• CAS NO: 4073-35-2
• Molecular Formula: C₈H₆Br₂O₃
• Molecular Weight: 309.94
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 4073-35-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: 224 °C
• Boiling Point: 365.2 °C at 760 mmHg
• Flash Point: 174.7 °C
• Appearance: /
• Density: 1.957 g/cm³
• Vapor Pressure: 5.64E-06mmHg at 25°C
• Refractive Index: 1.614
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 3.69±0.10(Predicted)
• CAS DataBase Reference: 3,5-DIBROMO-4-METHOXYBENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIBROMO-4-METHOXYBENZOIC ACID(4073-35-2)
• EPA Substance Registry System: 3,5-DIBROMO-4-METHOXYBENZOIC ACID(4073-35-2)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 4073-35-2(Hazardous Substances Data)

Usage

General Description

3,5-Dibromo-4-methoxybenzoic Acid is a chemical compound that falls under the category of a bromobenzoic acid. 3,5-DIBROMO-4-METHOXYBENZOIC ACID contains two bromine atoms (dibromo), a methoxy group (-OCH3) located on the fourth carbon of the benzene ring, and a carboxylic acid group (-COOH). Its systematic name is 3,5-dibromo-4-methoxybenzoic acid and the CAS Registry Number for the compound is 6358-64-1. It has a molar mass of 329.93 g/mol. 3,5-DIBROMO-4-METHOXYBENZOIC ACID is usually used in academic and industrial chemical research and it's not typically found in consumer products. It has potential uses in the development of pharmaceutical and other specialty chemical applications.

InChI:InChI=1/C8H6Br2O3/c1-13-7-5(9)2-4(8(11)12)3-6(7)10/h2-3H,1H3,(H,11,12)

Upstream product

• 41727-47-3 methyl 3,5-dibromo-4-hydroxybenzoate 
• 100-09-4 4-methoxybenzoic acid 
• 64-19-7 acetic acid 
• 854692-55-0 2-bromo-1-(3,5-dibromo-4-methoxy-phenyl)-propan-1-one 
• 7697-37-2 nitric acid 
• 22812-61-9 methyl 3,5-dibromo-4-methoxybenzoate 
• 7726-95-6 bromine 
• 7732-18-5 water 
• 123-11-5 4-methoxy-benzaldehyde 
• 79324-79-1 1-(3,5-dibromo-4-methoxyphenyl)ethanone 
• 3337-62-0 3,5-dibromo-4-hydroxybenzoic acid 

Downstream Products

• 4319-02-2 4-O-methylgallic acid 
• 120-80-9 benzene-1,2-diol 
• 108-95-2 phenol 
• 1414518-14-1 (Z)-5-(3-bromo-4-hydroxybenzylidene)-4-(3-bromo-4-hydroxyphenyl)-3-(3,5-dibromo-4-hydroxybenzoyl)furan-2(5H)-one 
• 1563242-92-1 2-((3,5-dibromo-4-methoxybenzoyl)oxy)-N,N,N-trimethylethanaminium chloride 
• 114194-99-9 2-(3,5-Dibromo-4-methoxy-phenyl)-5-hydroxy-benzofuran-3-carboxylic acid ethyl ester 
• 114194-97-7 3,5-Dibromo-4-methoxybenzoylacetic acid ethyl ester 
• 488-48-2 tetrabromobenzoquinone 
• 607-99-8 2,4,6-tribromoanisole 
• 615-58-7 2,4-dibromophenol 

Relevant articles and documents

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N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY

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Steric Enhancement of Resonance-Evidence from Kinetic Study on some Acetophenones

The kinetics of oxidation of some mono-, di- and tri-substituted acetophenones by alkaline hexacyanoferrate(III) in 50percent (v/v) methanol-water mixture at constant ionic strength and at 20, 30 and 40 deg have been studied spectrophotometrically and the rate constants determined by least-squares analysis.Electron-withdrawing groups in the ring facilitate the oxidation of the acetyl function while electron-releasing groups retard the rate.The rate constant values for the oxidation of 3-substituted-4-alkoxy-acetophenones are computed based on the principle of additivity of group effects.The observed rate constants are significantly lower than the calculated values.This is attributed to the phenomenon of steric enhancement of resonance (SER). 3,5-Disubstituted-4-methoxyacetophenones have higher observed rate constant values than the calculated ones.The steric inhibition of resonance (SIR) operates in these systems.In the case of 3-halogeno-4-methoxyacetophenones, the importance of SER increases with increase in the bulkiness of the 3-substituents.The difference between the calculated and observed multiple substituent constants of 3-substituted-4-methoxyacetophenones also lends support for SER.