112641-64-2

Usage

Uses

Used in Research and Development:
6-Chloro-2-fluoro-3-methoxybenzaldehyde is utilized as a valuable research chemical, contributing to the advancement of scientific knowledge and the development of new materials and compounds.
Used in Chemical Synthesis:
6-Chloro-2-fluoro-3-methoxybenzaldehyde is used as an intermediate in the synthesis of various chemicals, including solvents, which are essential in the production of a wide range of products.
Used in Paints and Coatings Industry:
In the paints and coatings industry, 6-chloro-2-fluoro-3-methoxybenzaldehyde is used as a solvent for intermediate steps, aiding in the creation of high-quality paints with desired properties.
Used in Plastics Industry:
6-CHLORO-2-FLUORO-3-METHOXYBENZALDEHYDE is also employed in the plastics industry, where it serves as a solvent in the intermediate stages of plastic production, contributing to the development of innovative and improved plastic materials.
Used in Synthetic Resins Industry:
6-Chloro-2-fluoro-3-methoxybenzaldehyde is used as a solvent in the intermediate steps for the production of synthetic resins, which are crucial components in various applications, such as coatings, adhesives, and composites.
Used in Dyes Industry:
In the dyes industry, 6-CHLORO-2-FLUORO-3-METHOXYBENZALDEHYDE is utilized as a solvent in the intermediate stages of dye production, enabling the creation of a diverse range of colors and hues.
Used in Perfumery:
6-Chloro-2-fluoro-3-methoxybenzaldehyde is used in the manufacture of perfumes, where it contributes to the development of unique and complex fragrances.
Used in Solvents and Flavorings Industry:
6-CHLORO-2-FLUORO-3-METHOXYBENZALDEHYDE is also employed in the production of solvents and flavorings, where its chemical properties are harnessed to create a variety of products with specific characteristics and applications.

Upstream product

• 2591-86-8 N-Formylpiperidine 
• 452-09-5 4-chloro-2-fluoro-1-methoxybenzene 
• 321-28-8 1-fluoro-2-methoxybenzene 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 1308661-78-0 2-(3-{[(6-chloro-2-fluoro-3-methoxy-benzyl)-((S)-1-dimethylaminomethyl-3,3-dimethyl-butyl)-amino]-methyl}-benzyl)-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid((1R,2R,3R,5S)-2,6,6-trimethyl-bicyclo[3.1.1]hept-3-yl)-amide 
• 1308662-40-9 2-(3-{[(6-chloro-2-fluoro-3-methoxy-benzyl)-((S)-1-dimethylaminomethyl-3,3-dimethyl-butyl)-amino]-methyl}-5-dimethylamino-benzyl)-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid methyl ester 
• 1308662-44-3 2-(3-{[(6-chloro-2-fluoro-3-methoxy-benzyl)-((S)-1-dimethylaminomethyl-3,3-dimethyl-butyl)-amino]-methyl}-5-dimethylamino-benzyl)-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid ethyl ester 
• 1308661-80-4 2-(3-{[(6-chloro-2-fluoro-3-methoxy-benzyl)-((S)-1-dimethylaminomethyl-2-phenyl-ethyl)-amino]-methyl}-benzyl)-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid ((1S,2S,3S,5R)-2,6,6-trimethyl-bicyclo[3.1.1]hept-3-yl)-amide 
• 1308661-81-5 2-[3-({(6-chloro-2-fluoro-3-methoxy-benzyl)-[(S)-2-(3-chloro-phenyl)-1-dimethylaminomethyl-ethyl]-amino}-methyl)-benzyl]-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid((1S,2S,3S,5R)-2,6,6-trimethyl-bicyclo[3.1.1]hept-3-yl)-amide 
• 1308661-82-6 2-[3-({(6-chloro-2-fluoro-3-methoxy-benzyl)-[(S)-2-(4-chloro-phenyl)-1-dimethylaminomethyl-ethyl]-amino}-methyl)-benzyl]-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid((1S,2S,3S,5R)-2,6,6-trimethyl-bicyclo[3.1.1]hept-3-yl)-amide 
• 1308662-17-0 2-(3-{[(6-Chloro-2-fluoro-3-methoxy-benzyl)-((S)-1-dimethylaminomethyl-3,3-dimethyl-butyl)-amino]-methyl}-benzyl)-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid ethyl ester 
• 1308662-42-1 2-(3-{[(6-Chloro-2-fluoro-3-methoxy-benzyl)-((S)-1 dimethylaminomethyl-3,3-dimethyl-butyl)-amino]-methyl}-benzyl)-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid 

Relevant academic research and scientific papers

Design and application of a low-temperature continuous flow chemistry platform

A flow reactor platform technology applicable to a broad range of low temperature chemistry is reported. The newly developed system captures the essence of running low temperature reactions in batch and represents this as a series of five flow coils, each with independently variable volume. The system was initially applied to the functionalization of alkynes, Grignard addition reactions, heterocycle functionalization, and heteroatom acetylation. This new platform has then been used in the preparation of a 20-compound library of polysubstituted, fluorine-containing aromatic substrates from a sequential metalation-quench procedure and can be readily adapted to provide gaseous electrophile inputs such as carbon dioxide using a tube-in-tube reactor.

SULTAM DERIVATIVES

The present invention relates to compounds according to formula 1, which exhibit cytotoxic activity. The compounds may be used in the treatment of cancer.

Synthesis and evaluation of the anti-mammary tumor activity and of the estrogenic side effects of platinum(II) complexes

The synthesis and structural characterization of mammary tumor-inhibiting, diastereomeric platinum(II) complexes with 2,6-Cl2, 2F, 6-Cl, 2-Cl, 6-F and 2,6-F2 substituents (1-PtSO4 to 4-PtSO4) are describ

Dihydropyridine derivatives, processes for their preparation and pharmaceutical compositions thereof

There are described compounds of Formula I, in which R1, R2, R3 and R4 are as defined in the specification,R5 is alkyl optionally interrupted by an amide group and optionally substituted by halogen or by a carboxy or a heterocyclic group,X is -O-, -NR-, -S(O)m1, or a bond,Z is hydrogen or together with R forms a bond,R is hydrogen, alkyl or together with Z forms a bond,R6 is a 5 or 6 membered unsaturated nitrogen containing heterocyclic ring, optionally fused to a phenyl ring and optionally substituted by one or more of oxo, hydroxy, alkyl, -(CH2)n1NH2, alkoxy, phenyl or -COOH,and when X is -NR- or -S(O)m1-, R6 may in addition be hydrogen or a group -CH2CH2NH2, -CH2CH2-het. or NHC(=NH)NH2,when X is -O-, R6 may also be a group -NH2, -C(=O) (CH2)nNH2, -CH2CH2NR14R15 or CH2CH2OCH2CH2NR14R15,when X is -NR-, -S(O)m1-, or a bond, R6 may also be hydrogen or a group -C(=NR12)NHR13,R13 and R14 may be hydrogen or alkyl,R12 is hydrogen, alkylcarbonyl, nitrile or hydroxy,R15 is hydrogen or a group R11,m and m1 are each 0, 1 or 2,n is 0 or 1,n1 is an integer from 0 to 6, and pharmaceutically acceptable salts, esters, amides, analogues and protected derivatives thereof.