203573-09-5

Basic information

• Product Name: Benzoic acid, 3,5-dichloro-4-Methyl-, Methyl ester
• Synonyms: Benzoic acid, 3,5-dichloro-4-Methyl-, Methyl ester;methyl 3,5-dichloro-4-methylbenzoate
• CAS NO: 203573-09-5
• Molecular Formula: C9H8Cl2O2
• Molecular Weight: 219.06462
• Mol File: 203573-09-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 293.9±35.0 °C(Predicted)
• Appearance: /
• Density: 1.307±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzoic acid, 3,5-dichloro-4-Methyl-, Methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3,5-dichloro-4-Methyl-, Methyl ester(203573-09-5)
• EPA Substance Registry System: Benzoic acid, 3,5-dichloro-4-Methyl-, Methyl ester(203573-09-5)

Safety Data

• Hazardous Substances Data: 203573-09-5(Hazardous Substances Data)

Usage

General Description

Benzoic acid, 3,5-dichloro-4-methyl-, methyl ester is a chemical compound that is often used in the manufacturing of various products such as perfumes, soaps, and flavorings. It is also used as a preservative in the food and beverage industry due to its antimicrobial properties. Benzoic acid, 3,5-dichloro-4-Methyl-, Methyl ester is known for its ability to inhibit the growth of bacteria and fungi, making it an effective ingredient in cosmetic and personal care products. Additionally, it is used in the production of pharmaceuticals and agricultural chemicals. Overall, benzoic acid, 3,5-dichloro-4-methyl-, methyl ester is a versatile compound with a wide range of applications in various industries.

Upstream product

• 203573-15-3 methyl 2,3,5-trichloro-4-methylbenzoate 
• 12775-96-1 copper 
• 67-56-1 methanol 
• 39652-34-1 3,5-dichloro-4-methylbenzoic acid 

Downstream Products

• 1465326-89-9 methyl 3,5-dichloro-4-formylbenzoate 
• 859212-75-2 methyl 4-(bromomethyl)-3,5-dichlorobenzoate 

Relevant articles and documents

Efficient three-component synthesis of diversely substituted tetrahydro-1H-cyclopenta[c]quinolines

The synthesis of highly functionalized substituted tetrahydro-1H-cyclopenta[c]quinoline (I) and its reduced derivatives hexahydro-1H-cyclopenta[c]quinolines (II) via Povarov reaction in high diastereoselectivity and high to moderate yields is described he

SUBSTITUTED TRICYCLIC COMPOUNDS WITH ACTIVITY TOWARDS EP1 RECEPTORS

The present invention belongs to the field of EP1 receptor ligands. More specifically it refers to compounds of general formula (I) having great affinity and selectivity for the EP1 receptor. The invention also refers to the process for their preparation, to their use as medicament for the treatment and/or prophylaxis of diseases or disorders mediated by the EP1 receptor as well as to pharmaceutical compositions comprising them.

Method for preparing aromatic compounds

A method for synthesizing aromatic compounds by selectively dehalogenating aromatic starting materials is provided. Compounds may be prepared which are substituted with fluoro, chloro or bromo. The method may be used to remove halogen atoms from sites at which halogenation is not desired, and to form substantially pure halogenated compounds from mixtures of starting materials. The method uses a copper containing dehalogenation agent and an acid with the dehalogenation being controlled by a substituent such as a carboxylic acid, amide, ester, aldehyde, ketone or cyano on the aromatic ring.