36335-47-4

Basic information

• Product Name: 3-CHLORO-2,6-DIMETHOXYBENZOIC ACID, 97
• Synonyms: 3-CHLORO-2,6-DIMETHOXYBENZOIC ACID, 97
• CAS NO: 36335-47-4
• Molecular Formula: C₉H₉ClO₄
• Molecular Weight: 216.619
• Mol File: 36335-47-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 131-133°C
• Appearance: /
• CAS DataBase Reference: 3-CHLORO-2,6-DIMETHOXYBENZOIC ACID, 97(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLORO-2,6-DIMETHOXYBENZOIC ACID, 97(36335-47-4)
• EPA Substance Registry System: 3-CHLORO-2,6-DIMETHOXYBENZOIC ACID, 97(36335-47-4)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 36335-47-4(Hazardous Substances Data)

Usage

General Description

3-Chloro-2,6-dimethoxybenzoic acid, also known as 3,5-dimethoxy-4-chlorobenzoic acid, is a chemical compound that is mainly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is a white to off-white crystalline solid with a molecular formula C9H9ClO4. The compound is a derivative of benzoic acid and is characterized by the presence of a chlorine atom and two methoxy groups on the benzene ring. It is commonly used in research and development and has applications in the fields of medicine and agriculture due to its potential as a building block for the synthesis of biologically active molecules. The 97% purity level indicates that it is highly pure and suitable for use in various chemical reactions and processes.

Upstream product

• 2040-04-2 2,6-dimethoxyacetophenone 
• 1466-76-8 2-6-dimethoxybenzoic acid 

Downstream Products

• 26754-77-8 3-chloro-2,6-dihydroxy-benzoic acid 
• 36335-48-5 3-chloro-2,6-dimethoxybenzoyl chloride 
• 73219-92-8 3-bromo-5-chloro-2,6-dimethoxybenzoic acid 
• 106567-17-3 3-Chloro-2,6-dimethoxy-N,N-dimethyl-benzamide 
• 82977-52-4 (-)-A 32507 
• 89653-83-8 3-Bromo-5-chloro-2,6-dimethoxy-benzoyl chloride 
• 82935-27-1 A 32637 
• 82935-44-2 (-)-N-ethyl-2-(3-chloro-2,6-dimethoxybenzamidomethyl)pyrrolidine 
• 130880-18-1 3-chloro-6-methoxy-N-(1-benzyl-4-piperidinyl)salicylamide 
• 130880-08-9 2,6-dimethoxy-3-chloro-N-(1-benzyl-4-piperidinyl)benzamide 
• 130880-19-2 3-Chloro-2-hydroxy-6-methoxy-N-[1-(4-methyl-benzyl)-piperidin-4-yl]-benzamide 
• 130880-09-0 3-Chloro-2,6-dimethoxy-N-[1-(4-methyl-benzyl)-piperidin-4-yl]-benzamide 
• 95-88-5 4-Chlororesorcinol 
• 717854-91-6 N-[1-acetyl-5,7-dimethoxy-4-(4-methoxyphenyl)-2,2,4-trimethyl-1,2,3,4-tetrahydroquinolin-6-yl]-3-chloro-2,6-dimethoxybenzamide 

Relevant articles and documents

Efficient halogenation synthesis method of aryl halide

The invention discloses an efficient halogenation synthesis method of aryl halide. The method comprises the following step: in the presence of a catalyst (sulfoxide or oxynitride), a halogenation reagent and a solvent, carrying out a halogenation reaction on an aromatic ring compound to obtain the aryl halide. According to the present invention, in the presence of a catalyst (sulfoxide or nitrogenoxide), a halogenation reagent and a solvent, the aromatic ring is subjected to an efficient halogenation reaction, such that the very useful aryl halide can be obtained with high activity and high selectivity; and by adopting the method disclosed by the invention, aryl halides can be efficiently synthesized, and the method has a wide application prospect in actual production.

Chromatographic Separation of Enantiomers and Barriers to Enantiomerization of Axially Chiral Aromatic Carboxamides

The enantiomers (M) and (P) of a series of similar aromatic carboxamides have been, for the first time, investigated analytically and enriched preparatively by liquid chromatography on triacetylcellulose.Enantiomeric purities (7-99percent), specific rotations, and barriers to rotation about the C(sp2)-C(sp2) bond (87 - 120 kJ/mol, Table 5) were determined.These energies are discussed in terms of the size of ortho substituents and of the buttressing effects by meta substituents.

2,6-Dialkoxybenzamides, intermediates, pharamaceutical compositions and methods for treatment of psychotic disorders

A compound of the formula, wherein R1 is an alkyl group with 1-3 carbon atoms, R2 and R3 are the same or different and each is hydrogen, chlorine or bromine; and pharmaceutically acceptable salts and optical isomers thereof; methods and intermediates for