72482-14-5

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2,4-DIMETHOXY-3-CHLOROBENZALDEHYDE is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products.
Used in Dyes and Pigments Production:
2,4-DIMETHOXY-3-CHLOROBENZALDEHYDE is used as a raw material in the production of dyes and pigments, playing a crucial role in the creation of vibrant colors for various applications.
Used in Flavors and Fragrances Industry:
Leveraging its aromatic properties, 2,4-DIMETHOXY-3-CHLOROBENZALDEHYDE is utilized in the manufacture of flavors and fragrances, enhancing the sensory experience of various consumer products.
It is important to handle 2,4-DIMETHOXY-3-CHLOROBENZALDEHYDE with care due to potential health risks, and it should be used in a controlled environment to ensure safety.

Upstream product

• 4885-02-3 Dichloromethyl methyl ether 
• 7051-15-2 2-chlororesorcinol dimethyl ether 
• 131088-00-1 3-chloro-2,4-dihydroxylbenzaldehyde 
• 74-88-4 methyl iodide 

Downstream Products

• 914933-75-8 3-chloro-2,4-dimethoxybenzoic acid 
• 791-28-6 Triphenylphosphine oxide 
• 502483-92-3 3-(3-chloro-2,4-dimethoxyphenyl)acrylic acid 
• 90247-27-1 (R)-3-[(S)-8-Chloro-3-(2-fluoro-phenyl)-5,6-dihydro-furo[2',3':4,5]benzo[1,2-d]isoxazole-6-carbonyl]-4-phenyl-oxazolidin-2-one 
• 90247-26-0 (R)-3-[(R)-8-Chloro-3-(2-fluoro-phenyl)-5,6-dihydro-furo[2',3':4,5]benzo[1,2-d]isoxazole-6-carbonyl]-4-phenyl-oxazolidin-2-one 
• 90247-30-6 (S)-8-Chloro-3-(2-fluoro-phenyl)-5,6-dihydro-furo[2',3':4,5]benzo[1,2-d]isoxazole-6-carboxylic acid 
• 90247-29-3 (R)-8-Chloro-3-(2-fluoro-phenyl)-5,6-dihydro-furo[2',3':4,5]benzo[1,2-d]isoxazole-6-carboxylic acid 
• 90247-08-8 8-chloro-3-(2-fluorophenyl)-5,6-dihydrofuro[3,2-f]-1,2-benzisoxazole-6-carboxylic acid 
• 90246-99-4 ethyl (E)-7-chloro-2,3-dihydro-5-(o-fluorobenzoyl)-6-hydroxybenzofuran-2-carboxylate O-acetyloxime 
• 90246-88-1 ethyl (E)-7-chloro-2,3-dihydro-5-(o-fluorobenzoyl)-6-hydroxybenzofuran-2-carboxylate oxime 
• 90246-98-3 ethyl 8-chloro-5,6-dihydro-3-(o-fluorophenyl)furo[3,2-f]-1,2-benzisoxazole-6-carboxylate 
• 90246-78-9 ethyl 7-chloro-2,3-dihydro-5-(o-fluorobenzoyl)-6-hydroxybenzofuran-2-carboxylate 
• 90247-25-9 8-chloro-5,6-dihydro-3-(o-fluorophenyl)furo<3,2-f>-1,2-benzisoxazole-6-carbonyl chloride 
• 90247-23-7 8-chloro-5,6-dihydro-3-(o-fluorophenyl)furo[3,2-f]-1,2-benzisoxazole-6-carboxamide 

Relevant academic research and scientific papers

5-METHYL-6-PHENYL-4,5-DIHYDRO-2H-PYRIDAZIN-3-ONE DERIVATIVE

The present invention provides an agent for treating malignant tumor, comprising a compound of formula (1): wherein R1 to R4 are hydrogen atom, halogen, or etc., Y is optionally-substituted alkylene group or etc.

Mild synthesis of asymmetric 2′-carboxyethyl-substituted fluoresceins

(Chemical Equation Presented) Asymmetric fluoresceins bearing a carboxyethyl group in the chromophoric portion of the dyes were prepared by a reaction of substituted phthalic anhydride with a carboxyethyl substituted resorcinol analogue followed by a condensation with a second resorcinol analogue. In order to avoid an accumulation of symmetric side products, the second step was performed in two substeps: acid-catalyzed formation of a triphenylmethyl intermediate followed by base-catalyzed cyclization which furnished the desired dyes.

Total synthesis of topopyrones B and D

(Chemical Equation Presented) We describe a straightforward synthesis of topopyrones B and D, which are potent and selective inhibitors of topoisomerase I. The chemistry should be suitable for additional structure-activity relationship (SAR) work.

1,2-benzisoxazoloxyacetic acids and related compounds

Novel 1,2-benzisoxazoloxyacetic acids and related compounds, methods for preparing same and methods of treatment by administering compositions containing such a compound are described. These compounds are useful as diuretic, uricosuric and antihypertensive agents.

Substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazole-6-carboxylic acids: High-ceiling diuretics with uricosuric activity

A series of substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazoles was prepared and evaluated for their saluretic and uricosuric properties. Pharmacological evaluation of the title compounds was carried out in mice, rats, dogs, and monkeys. The diuretic/sa

Benzisoxazole carboxylic acids

Described are compounds of the formula STR1 wherein X is hydrogen, loweralkyl, halo, loweralkoxy or trifluoromethyl, and Z is hydrogen, loweralkyl, halo, hydroxy or alkoxy, or compounds of the formula STR2 wherein X' and Y' may be the same or different an

Benzisoxazole carboxylic acids

Described are compounds of the formula STR1 wherein X is hydrogen, loweralkyl, halo, loweralkoxy or trifluoromethyl, and Z is hydrogen, loweralkyl, halo, hydroxy or alkoxy, or compounds of the formula STR2 wherein X' and Y' may be the same or different an