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Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-4,5-dimethoxybenzoic acid 97 is used as an intermediate in the synthesis of various pharmaceuticals for its ability to introduce the 3-chloro-4,5-dimethoxyphenyl group into molecules, which can enhance the therapeutic properties of the resulting compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 3-chloro-4,5-dimethoxybenzoic acid 97 is utilized as an intermediate in the production of various agrochemicals, contributing to the development of effective and innovative products for agricultural applications.
Used as a Reagent in Organic Synthesis:
3-Chloro-4,5-dimethoxybenzoic acid 97 is used as a reagent in organic synthesis to introduce the 3-chloro-4,5-dimethoxyphenyl group into molecules, which can improve the chemical and biological properties of the synthesized compounds.
Used in Research and Development:
3-Chloro-4,5-dimethoxybenzoic acid 97 is used in research and development for its potential anti-inflammatory and anti-cancer properties, with ongoing studies aimed at exploring its therapeutic potential and applications in medicine.
Overall, 3-chloro-4,5-dimethoxybenzoic acid 97 is a versatile and valuable chemical compound with diverse applications across various industries, particularly in the development and synthesis of pharmaceuticals and agrochemicals, as well as in organic synthesis and research.

InChI:InChI=1/C9H9ClO4/c1-13-7-4-5(9(11)12)3-6(10)8(7)14-2/h3-4H,1-2H3,(H,11,12)

Upstream product

• 93-07-2 Veratric acid 
• 90537-30-7 5-chloro-3,4-dimethoxybenzonitrile 
• 18268-68-3 5-chloroveratraldehyde 

Downstream Products

• 1181450-42-9 C₉H₈Cl₂O₃ 
• 1431546-26-7 tert-butyl (3-(1-(3-chloro-4,5-dimethoxybenzoyl)piperidin-4-yl)benzyl)carbamate 
• 94250-90-5 3-chloro-4,5-dimethoxy-benzoic acid-(2-diethylamino-ethyl ester); hydrochloride 
• 132496-77-6 methyl 3,4-dihydroxy-5-chlorobenzoate 
• 132496-78-7 Methyl 5-chloro-3,4-di-p-methoxybenzyloxybenzoate 
• 1338708-61-4 3-chloro-4,5-bis((4-methoxybenzyl)oxy)-N-(2-(pyrrolidin-1-yl)ethyl)benzamide 
• 1623785-45-4 2-(3-chloro-4,5-dimethoxybenzyl)-7-methoxy-6-(triisopropylsilyloxy)-1,2,3,4-tetrahydroisoquinoline 

Relevant academic research and scientific papers

Synthesis and biological activities of new halophenols

A series of new halophenols were synthesized, and their structures were established on the basis of 1H, 13C NMR and mass spectral data. All of the prepared compounds were screened for their in vitro protein tyrosine kinase (PTK) and vascular smooth muscle cell (VSMC) proliferation inhibitory activity. Twelve halophenols showed significant PTK inhibitory activity, most of them exhibited stronger activities than that of genistein, a positive reference compound. Several halophenols also displayed moderate VSMC proliferation inhibitory activity, compound 8c showed higher activity than that of tetrandrine, a positive reference compound. The preliminary structure-activity relationships of these compounds were investigated and discussed. The results provided a foundation for the action mechanism study and further structure optimization of the halophenols.

Studies on Pitch Problems Caused by Pulping and Bleaching of Tropical Woods. XIV. Chemistry of the Aurone Derivatives at the Conventional Bleaching Stages

Rengasin (1), which is responsible for the colored specks on a sheet of bleached sulfate pulp from the woods of rengas (Anacardiaceae), was converted into R1 7 having a novel carbon skeleton.A closely related analogue, S1 8, prepared from sulfuretin (2) was used as a model to investigate further conversions under bleaching conditions.Chlorination of S1 8 produced an equilibrium mixture involving compound 9 as a dominant compound.The latter was transformed by the treatment with chlorine dioxide into an orthoquinone (16) via two pathway containing 10 in one and 15 in another.The monomeric quinone (16) immediately dimerized in acidic media to give 20 under the same conditions as above, and the further oligomerization by the process similar to that in dimerization of 16 finally afforded a mixture of colored oligomers 26.