620621-48-9

Basic information

• Product Name: 2-CHLORO-5-IODOBENZOIC ACID METHYL ESTER
• Synonyms: 2-CHLORO-5-IODOBENZOIC ACID METHYL ESTER;METHYL 2-CHLORO-5-IODOBENZOATE;2-Chloro-5-iodoobenzoic acid Methyl ester
• CAS NO: 620621-48-9
• Molecular Formula: C₈H₆ClIO₂
• Molecular Weight: 296.49
• Product Categories: Acids & Esters;Chlorine Compounds;Iodine Compounds
• Mol File: 620621-48-9.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 315 °C at 760 mmHg
• Flash Point: 144.3 °C
• Appearance: /
• Density: 1.837±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0.00045mmHg at 25°C
• Refractive Index: 1.608
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 2-CHLORO-5-IODOBENZOIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-5-IODOBENZOIC ACID METHYL ESTER(620621-48-9)
• EPA Substance Registry System: 2-CHLORO-5-IODOBENZOIC ACID METHYL ESTER(620621-48-9)

Safety Data

• Hazardous Substances Data: 620621-48-9(Hazardous Substances Data)

Usage

General Description

2-Chloro-5-iodobenzoic acid methyl ester is a chemical compound with the molecular formula C8H6ClIO2. It is a derivative of benzoic acid and is classified as an ester due to its functional group. 2-CHLORO-5-IODOBENZOIC ACID METHYL ESTER is a white to off-white solid with a molecular weight of 292.49 g/mol. It is commonly used in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. 2-Chloro-5-iodobenzoic acid methyl ester is also known for its potential applications in the field of medicinal chemistry and drug discovery due to its structural and pharmacological properties. Additionally, it is important to handle this compound with caution as it may pose health hazards and environmental risks. Overall, 2-Chloro-5-iodobenzoic acid methyl ester is a versatile chemical that has various industrial and research applications.

InChI:InChI=1/C8H6ClIO2/c1-12-8(11)6-4-5(10)2-3-7(6)9/h2-4H,1H3

Upstream product

• 67-56-1 methanol 
• 19094-56-5 2-chloro-5-iodobenzoic acid 
• 75-36-5 acetyl chloride 
• 637-87-6 1-Chloro-4-iodobenzene 

Downstream Products

• 792911-91-2 methyl 2-chloro-5-((trimethylsilyl)ethynyl)benzoate 
• 1143024-76-3 methyl 2-chloro-5-cyclopent-2-enyl-benzoate 
• 1143025-42-6 methyl 2-chloro-5-(4-(dimethylamino)piperidin-1-yl)benzoate 
• 1143025-49-3 methyl 2-chloro-5-(3-(diethylamino)pyrrolidin-1-yl)benzoate 
• 1143024-49-0 methyl 2-chloro-5-(pyridin-2-yl)benzoate 
• 1394348-61-8 2-chloro-5-(pyridin-3-yloxy)benzoic acid methyl ester 
• 1394348-59-4 sodium 2-chloro-5-(pyridin-4-yloxy)benzoate 
• 1394346-77-0 2-chloro-5-(pyrimidin-4-ylamino)-benzoic acid methyl ester 
• 1394348-47-0 2-chloro-5-(2-methyl-2H-pyrazol-3-ylamino)-benzoic acid methyl ester 
• 1143024-51-4 2-chloro-5-pyridin-2-ylbenzoic acid 
• 1143023-55-5 2-chloro-5-ethyl-N-(6-(3-(4-methylpiperazin-1-yl)propylsulfonyl)benzo[d]thiazol-2-ylcarbamoyl)benzamide 
• 1143024-61-6 2-chloro-5-ethynylbenzoic acid 
• 1143020-09-0 2-chloro-5-ethynylbenzamide 
• 1143023-36-2 2-chloro-5-ethynyl-N-[[6-[3-(4-methylpiperazin-1-yl)propylsulfonyl]benzothiazol-2-yl]carbamoyl]benzamide 

Relevant articles and documents

Tunable aryl imidazolium ionic liquids (TAIILs) as environmentally benign catalysts for the esterification of fatty acids to biodiesel fuel

Herein, we describe the synthesis of tunable aryl imidazolium ionic liquid catalysts and tested for esterification of fatty acids to biodiesel. In this work, six tunable aryl imidazolium ionic liquids (TAIILs) 1a-1f were prepared. These ionic liquids were used as the economical and reusable catalysts for the synthesis of biodiesel fuels. The reaction has been preceded in a monophase at 80 °C for 4 h, after which the product was separated from the catalyst system by a simple liquid/liquid phase separation at room temperature with excellent yields. With the simple post-process, the catalyst is reusable at least 6 times. This novel method offers a short reaction time, good yields, and environmentally benign characteristics.

Synthesis and biological activity of benzamides substituted with pyridine-linked 1,2,4-oxadiazole

To find pesticidal lead compounds with high activity, a series of novel benzamides substituted with pyridine-linked 1,2,4-oxadiazole were designed by bioisosterism, and synthesized easily via esterification, cyanation, cyclization and aminolysis reactions

Novel bifenthrin derivatives, and preparation method and application thereof

The invention discloses novel bifenthrin derivatives, and a preparation method and application thereof. The novel bifenthrin derivatives have a structural formula as shown in a formula (I) which is described in the specification. In the formula (I), when R1 is H, R2 is a Cl or CF3 substituent group, and R3 is H or a substituted or unsubstituted non-heterocyclic or heterocyclic aryl group; when R1is a Cl substituted group, R 2 is H or a Cl or CF3 substituent group, and R3 is H or a substituted or unsubstituted non-heterocyclic or heterocyclic aryl group; the non-heterocyclic aryl group is a phenyl, naphthyl, anthryl, phenanthryl or pyrenyl group; and the heterocyclic aryl group is a five-to-nine-membered monocyclic or polycyclic heterocyclic aryl group with one or more O or S heteroatoms.According to the invention, a series of the novel bifenthrin derivatives are synthesized mainly by modifying and transforming ortho-position and terminal-position benzene rings on the intermediate benzene rings of bifenthrin; and the novel bifenthrin derivatives have excellent insecticidal and mosquito-killing effect on both larvae and adult mosquitoes, are significantly reduced in toxicity and improved in metabolic stability, and shows good application prospects.