2905-68-2

Basic information

• Product Name: METHYL 3,4-DICHLOROBENZOATE
• Synonyms: RARECHEM AL BF 0536;METHYL 3,4-DICHLOROBENZENECARBOXYLATE;METHYL 3,4-DICHLOROBENZOATE;3,4-DICHLOROBENZOIC ACID METHYL ESTER
• CAS NO: 2905-68-2
• Molecular Formula: C₈H₆Cl₂O₂
• Molecular Weight: 205.04
• Product Categories: Aromatic Esters
• Mol File: 2905-68-2.mol
• Article Data: 20

Chemical Properties

• Melting Point: 44 °C
• Boiling Point: 264 °C at 760 mmHg
• Flash Point: 112.6 °C
• Appearance: /
• Density: 1.355 g/cm³
• Vapor Pressure: 0.00995mmHg at 25°C
• Refractive Index: 1.545
• CAS DataBase Reference: METHYL 3,4-DICHLOROBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3,4-DICHLOROBENZOATE(2905-68-2)
• EPA Substance Registry System: METHYL 3,4-DICHLOROBENZOATE(2905-68-2)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 2905-68-2(Hazardous Substances Data)

Usage

General Description

Methyl 3,4-Dichlorobenzoate is a synthetic, organic chemical compound that belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. Structurally, it comprises of a methyl ester functioning group bound to the carbon of a benzoic acid that is further substituted by two chlorine atoms at the 3rd and 4th position. It is represented with the molecular formula C8H6Cl2O2. As an industrial chemical, it could possibly be used in various applications, including in the synthesis of other compounds. However, information about its specific uses, safety, or toxicity is limited and should be handled with appropriate safety measures.

InChI:InChI=1/C8H6Cl2O2/c1-12-8(11)5-2-3-6(9)7(10)4-5/h2-4H,1H3

Upstream product

• 28394-58-3 3,4-dichloro-benzoic acid ethyl ester 
• 17287-03-5 trimethylsulphonium hydroxide 
• 51-44-5 3,4-dichlorbenzoic acid 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 
• 1805-32-9 3,4-dichlorobenzyl alcohol 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 6287-38-3 3,4-dichlorobenzaldehyde 
• 75-91-2 tert.-butylhydroperoxide 
• 89978-33-6 methyl 2,3,4-trichlorobenzoate 
• 107-06-2 1,2-dichloro-ethane 
• 3024-72-4 3,4-dichlorobenzoyl chloride 
• 598-99-2 Methyl trichloroacetate 

Downstream Products

• 2905-65-9 methyl 3-chlorobenzoate 
• 1333392-71-4 3,4-dichloro-[N'-(benzofuroxan-5-yl)methylene]benzohydrazide 
• 93534-22-6 1-(3,4-dichlorophenyl)-2-phenyl-ethan-1-one 
• 1250663-38-7 C₈H₇Cl₂NO₂ 
• 63105-53-3 methyl 3,4-dichloro-5-nitrobenzoate 
• 1805-32-9 3,4-dichlorobenzyl alcohol 
• 6287-38-3 3,4-dichlorobenzaldehyde 
• 127918-65-4 O-methyl 3,4-dichlorobenzenecarbothioate 

Relevant articles and documents

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Rational design strategies based on practical fluorescence modulation mechanisms would enable us to rapidly develop novel fluorescence probes for target molecules. Here, we present a practical and general principle for modulating the fluorescence properti

Site-Selective Cross-Coupling of Remote Chlorides Enabled by Electrostatically Directed Palladium Catalysis

Control of site-selectivity in chemical reactions that occur remote from existing functionality remains a major challenge in synthetic chemistry. We describe a strategy that enables three of the most commonly used cross-coupling processes to occur with high site-selectivity on dichloroarenes that bear acidic functional groups. We have achieved this by repurposing an established sulfonylated phosphine ligand to exploit its inherent bifunctionality. Mechanistic studies suggest that the sulfonate group engages in attractive electrostatic interactions with the cation associated with the deprotonated substrate, guiding cross-coupling to the chloride at the arene meta position. This counterintuitive combination of anionic ligand and anionic substrate demonstrates an alternative design principle when considering the application of noncovalent interactions to direct catalysis.

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