2905-69-3

Basic information

• Product Name: METHYL 2,5-DICHLOROBENZOATE
• Synonyms: RARECHEM AL BF 0427;METHYL 2,5-DICHLOROBENZOATE;LABOTEST-BB LT00847973;2,5-DICHLOROBENZOIC ACID METHYL ESTER;2,5-dichlorobenzoic;2,5-dichloro-benzoicacimethylester;2,5-dichlorobenzoic acid methyl ether
• CAS NO: 2905-69-3
• Molecular Formula: C₈H₆Cl₂O₂
• Molecular Weight: 205.04
• EINECS: 220-815-7
• Product Categories: Aromatic Esters;Benzoic acid;Acids & Esters;Chlorine Compounds;C8 to C9;Carbonyl Compounds;Esters
• Mol File: 2905-69-3.mol
• Article Data: 7

Chemical Properties

• Melting Point: 37-40 °C(lit.)
• Boiling Point: 265.176 °C at 760 mmHg
• Flash Point: >230 °F
• Appearance: /
• Density: 1.356 g/cm³
• Vapor Pressure: 0.0093mmHg at 25°C
• Refractive Index: 1.545
• Storage Temp.: Sealed in dry,Room Temperature
• BRN: 2251582
• CAS DataBase Reference: METHYL 2,5-DICHLOROBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2,5-DICHLOROBENZOATE(2905-69-3)
• EPA Substance Registry System: METHYL 2,5-DICHLOROBENZOATE(2905-69-3)

Safety Data

• Safety Statements: 23-24/25
• RIDADR: UN 3077 9 / PGIII
• WGK Germany: 3
• TSCA: Yes
• Hazardous Substances Data: 2905-69-3(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 2905-69-3 differently. You can refer to the following data:
1. Methyl 2,5-Dichlorobenzoate is used as a starting material in the preparations of polyphenylenes.
2. Methyl 2,5-dichlorobenzoate was used as starting reagent in the synthesis of poly(p-phenylene). It was used in isolation of microorganism degrading methyl benzoate, Burkholderia cepacia and its ability to degrade different methyl aromatic esters.

Definition

ChEBI: A methyl ester resulting from the formal condensation of the carboxy group of 2,5-dichlorobenzoic acid with methanol. It as used as a plant growth regulator and fungicide for grafting of grapevines.

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

Upstream product

• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 120-82-1 1,2,4-Trichlorobenzene 
• 50-79-3 2,5-dichlorobenzoic acid 
• 65-85-0 benzoic acid 
• 17287-03-5 trimethylsulphonium hydroxide 
• 35112-27-7 ethyl 2,5-dichlorobenzoate 
• 119267-70-8 Acetic acid 2-(2,5-dichloro-phenyl)-2-oxo-ethyl ester 

Downstream Products

• 2905-65-9 methyl 3-chlorobenzoate 
• 1918-00-9 3,6-dichloro-O-anisic acid 
• 34145-05-6 2,5-dichlorobenzyl alcohol 
• 99585-13-4 methyl 2-methyl-5-chlorobenzoate 
• 1353055-80-7 methyl 5-chloro-2-(phenylthio)benzoate 
• 50-79-3 2,5-dichlorobenzoic acid 
• 1353055-81-8 methyl 2-(1-adamantylthio)-5-chlorobenzoate 
• 1353055-82-9 methyl 2,5-bis(1-adamantylthio)benzoate 
• 936479-44-6 methyl 5-chloro-2-(trimethylstannanyl)benzoate 
• 67487-35-8 2,5-dichlorobenzhydrazide 
• 108463-24-7 2-(5-Chloro-2-methoxyphenyl)-5,6-dihydro-4H-naphtho<1,2-b>pyran-4-one 
• 171897-89-5 1-(2,5-Dichlorophenyl)-2,2-bis(methylsulfanyl)ethanone 
• 6156-25-8 tetrathioorthocarbonic acid tetramethyl ester 
• 108463-13-4 1-(2,5-Dichlorophenyl)-3-(1,2,3,4-tetrahydro-1-oxo-2-naphthalenyl)-1,3-propanedione 

Relevant articles and documents

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Electroreduction of organic compounds, 36 [1]. Electroreduction of chlorinated methyl benzoates

The preparative electroreduction of the three methyl monochlorobenzoates, the six methyl dichlorobenzoates, and methyl 2,3,4-trichlorobenzoate in different solvent-supporting electrolytes (SSE) was studied. The rate of the dechlorination, which is the main reaction, is dependent on the substitution pattern. Pronounced regioselectivity is therefore observed in case of the oligochloro derivatives. Hydrogenation of the benzene ring and reduction of the methoxycarbonyl group with formation of a hydroxymethyl group are observed as side-reactions. Quantum chemical calculations on the reaction mechanism were performed. The theoretical results are in accordance with the experimental observations.