7740-05-8

Usage

Uses

Used in Chemical Synthesis:
5-Chloro-2-hydroxy-3-methoxybenzaldehyde is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure, which includes a benzaldehyde group and functional groups such as chlorine, hydroxy, and methoxy, allows it to participate in a range of chemical reactions, facilitating the creation of diverse chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Chloro-2-hydroxy-3-methoxybenzaldehyde may be employed as a building block for the development of new drugs. Its aromatic aldehyde structure and functional groups can be utilized to create novel drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
5-Chloro-2-hydroxy-3-methoxybenzaldehyde could be used as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its organochloride nature and aromatic aldehyde structure may contribute to the development of effective and environmentally friendly agrochemical products.
Used in Dye and Pigment Industry:
5-Chloro-2-hydroxy-3-methoxybenzaldehyde may also find applications in the dye and pigment industry, where it can be used as a precursor for the synthesis of various dyes and pigments. The presence of functional groups in its structure allows for the creation of colored compounds with specific properties, suitable for use in various applications, such as textiles, plastics, and printing inks.
Used in Flavor and Fragrance Industry:
5-Chloro-2-hydroxy-3-methoxybenzaldehyde may be utilized in the flavor and fragrance industry as a starting material for the synthesis of unique and complex aroma compounds. Its aromatic aldehyde structure and functional groups can be manipulated to create novel fragrances and flavorings for use in various consumer products.

InChI:InChI=1/C8H7ClO3/c1-12-7-3-6(9)2-5(4-10)8(7)11/h2-4,11H,1H3

Upstream product

• 16766-30-6 4-Chloroguaiacol 
• 90-05-1 2-methoxy-phenol 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 

Downstream Products

• 86232-26-0 3-methoxy-2-hydroxy-5-chlorotoluene 
• 86232-28-2 5-chloro-2,3-dimethoxybenzaldehyde 
• 93716-96-2 2-benzothiazol-2-yl-4-chloro-6-methoxy-phenol 
• 486994-24-5 2-(benzyloxy)-5-chloro-3-methoxybenzaldehyde 
• 1448325-00-5 (E)-N′-(5-chloro-2-hydroxy-3-methoxybenzylidene)-3-hydroxy-2-naphthohydrazide 
• 1442465-79-3 (2E,5E)-2,5-bis(5-chloro-2-hydroxy-3-methoxybenzylidene)cyclopentanone 
• 1217895-90-3 C₂₀H₂₄ClNO₂ 
• 1364686-87-2 7-(3-benzyloxy-propoxy)-5-chloro-3-nitromethyl-3H-benzo[c][1,2]oxaborol-1-ol 
• 1364686-80-5 3-(3-benzyloxy-propoxy)-5-chloro-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)benzaldehyde 
• 1364686-73-6 trifluoro-methanesulfonic acid 2-(3-benzyloxy-propoxy)-4-chloro-6-formyl-phenyl ester 

Relevant academic research and scientific papers

Synthesis method 5 - halogeno-veratraldehyde

The invention belongs to the field of organic chemistry, and in particular relates 5 - to a method for synthesizing halogenated O-veratraldehyde by using 4 - halogenoylguaiacol as a raw material to obtain 2 -hydroxy -3 - methoxy -5 -halogenated mandelic a

A synthetic preparation method for small carbags hydrochloric acid

The present invention belongs to the field of organic chemistry, relates to a method of synthesizing berberine hydrochloride, comprising: S1: with 5-halo-o-quinoastearaldehyde and piperine ethylamine to obtain N- [2-(3,4-dimethoxyphenyl-5-yl) ethyl] -1- (5-halo-2,3-dimethoxybenzyl) methylimide; S2: to obtain 2- (3,4-diimoxyphenyl) -N- (5-bromo-2,3-dimethoxybenzyl) ethylamine; S3: to obtain 2-(3,4-dimethoxyphenyl) -N- (5-bromo-2 S4: to obtain 12-halogenated berberine derivative; S5: to obtain berberine. The present invention is free from the application of the by-product o-vanillin synthesis of o-resveratal raw material constraints, synthesis of 5- substitute o-resveratal and piperine ethylamine, and the use of the two preparation of berberine hydrochloride, with raw materials readily available, mild reaction conditions, easy to operate, high chemical yield, low cost and other advantages.

Imidazo ring PAR4 antagonist and medical applications thereof

The invention relates to an imidazo ring compound represented by formula (I) or formula (II), or a pharmaceutically acceptable salt or ester or solvate thereof. The compound disclosed by the inventioncan be used for preparing medicines for preventing or treating thromboembolic diseases.

SUBSTITUTED ARYLAMINE COMPOUNDS AND THEIR USE AS 5-HT6 MODULATORS

The invention relates to 5-HT6 receptor antagonists. Novel arylamine compounds having the formula: (see formula I) and pharmaceutically acceptable salts and/or esters thereof, wherein - n is 0, 1, 2, 3, or 4; - A, when present is a lower alkyl

SYNTHESIS OF 5-HALOGEN-SUBSTITUTED 2,3-DIHYDROXYPHENYLACETIC ACIDS, THEIR ESTERS, AND 2,3-DIMETHOXYPHENYLACETOHYDROXAMIC ACIDS

Many-stage general methods were developed for the synthesis of 5-bromo- or 5-chloro-substituted 2,3-dimethoxyphenylacetic acids from o-vanilin.Methods were also developed for their conversion into the corresponding hydroxamic acids, 2,3-dihydroxyphenylace