153478-14-9

Basic information

• Product Name: 2,4-dichloro-1,5-dimethoxy-3-methylbenzene
• Synonyms: 2,4-dichloro-1,5-dimethoxy-3-methylbenzene
• CAS NO: 153478-14-9
• Molecular Weight: 221.083
• Mol File: 153478-14-9.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 2,4-dichloro-1,5-dimethoxy-3-methylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dichloro-1,5-dimethoxy-3-methylbenzene(153478-14-9)
• EPA Substance Registry System: 2,4-dichloro-1,5-dimethoxy-3-methylbenzene(153478-14-9)

Safety Data

• Hazardous Substances Data: 153478-14-9(Hazardous Substances Data)

Usage

General Description

2,4-dichloro-1,5-dimethoxy-3-methylbenzene is a chemical compound consisting of a benzene ring with two chlorine atoms, two methoxy groups, and a methyl group attached to it. It is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also utilized in the production of dyes, pigments, and fragrance compounds. This chemical has been found to have moderate toxicity and should be handled with care. It is important to follow safety protocols and use proper protective equipment when working with this compound.

Upstream product

• 186581-53-3 diazomethane 
• 160582-64-9 2,4-dichloro-5-methoxy-3-methylphenol 
• 854646-47-2 3,5-dichloro-2,6-dimethoxy-4-methyl-benzoic acid methyl ester 
• 60620-09-9 3,5-dichloro-2,6-dimethoxy-4-methyl-benzoic acid 
• 151-10-0 1,3-Dimethoxybenzene 
• 50375-04-7 1,3-dichloro-4,6-dimethoxybenzene 
• 74-88-4 methyl iodide 
• 7664-93-9 sulfuric acid 
• 500887-70-7 2-(3,5-dichloro-2,6-dimethoxy-4-methyl-benzoyl)-3,5-dimethoxy-benzoic acid methyl ester 
• 857537-89-4 2-(3,5-dichloro-2,6-dimethoxy-4-methyl-benzoyl)-3,5,6-trimethoxy-benzoic acid methyl ester 
• 4179-19-5 1,3-dimethoxy-5-methylbenzene 
• 63992-61-0 4,6-dichloro-5-methylresorcinol 

Downstream Products

• 1453211-58-9 2-chloro-5-[(2,6-dichloro-3,5-dimethoxybenzyl)oxy]pyrimidine 

Relevant articles and documents

Investigation of Covalent Warheads in the Design of 2-Aminopyrimidine-based FGFR4 Inhibitors

Covalent kinase inhibitors are rapidly emerging as a class of therapeutics with clinical benefits. Herein we report a series of selective 2-aminopyrimidine-based fibroblast growth factor receptor 4 (FGFR4) inhibitors exploring different types of cysteine-

Nitrogen-containing fused ring compounds as well as preparation method and application thereof

The invention discloses nitrogen-containing fused ring compounds as well as a preparation method and application thereof. The nitrogen-containing fused ring compounds have a structure represented by aformula (I) shown in the description, wherein each grou

Pyrimidopyridone compounds having antitumor activity as well as preparation method and application of pyrimidopyridone compounds

The invention discloses pyrimidopyridone compounds having antitumor activity as well as a preparation method and application of the pyrimidopyridone compounds. The invention particularly discloses thedeuterated pyrimidopyridone compounds represented by a