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Usage

Uses

Used in Organic Synthesis:
DIETHYL-6-(4-CHLOROPHENOXY) HEXYLMALONATE is used as a key intermediate in organic synthesis for its ability to facilitate the formation of complex organic molecules. Its presence in reactions can lead to the creation of a wide range of chemical products, making it an essential component in the development of new compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DIETHYL-6-(4-CHLOROPHENOXY) HEXYLMALONATE is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be incorporated into the design of new drugs, potentially leading to the development of novel treatments and therapies.
Used in Chemical Research:
DIETHYL-6-(4-CHLOROPHENOXY) HEXYLMALONATE is also utilized in chemical research as a model compound for studying reaction mechanisms and exploring new synthetic pathways. Its reactivity and versatility make it a valuable tool for researchers looking to understand and innovate within the field of organic chemistry.
Used in Agrochemical Industry:
In the agrochemical industry, DIETHYL-6-(4-CHLOROPHENOXY) HEXYLMALONATE is used as a precursor in the synthesis of various agrochemicals, including pesticides and herbicides. Its role in these applications is crucial for the development of effective and environmentally friendly solutions for agricultural challenges.
Used in Dye and Pigment Industry:
DIETHYL-6-(4-CHLOROPHENOXY) HEXYLMALONATE is employed in the dye and pigment industry as a starting material for the production of various dyes and pigments. Its unique properties contribute to the creation of vibrant and stable colorants used in a wide range of applications, from textiles to plastics.

Upstream product

• 37136-99-5 1-((6-bromohexyl)oxy)-4-chlorobenzene 
• 105-53-3 diethyl malonate 

Downstream Products

• 828934-40-3 C₁₇H₂₃ClO₄ 
• 124083-20-1 (R)-(+)-etomoxir 
• 131844-19-4 Butyric acid (S)-8-(4-chloro-phenoxy)-2-hydroxy-2-hydroxymethyl-octyl ester 
• 131844-19-4 Butyric acid (R)-8-(4-chloro-phenoxy)-2-hydroxy-2-hydroxymethyl-octyl ester 
• 124083-23-4 {(R)-2-[6-(4-Chloro-phenoxy)-hexyl]-oxiranyl}-methanol 
• 124083-18-7 {(S)-2-[6-(4-Chloro-phenoxy)-hexyl]-oxiranyl}-methanol 
• 131844-17-2 Butyric acid 2-butyryloxymethyl-8-(4-chloro-phenoxy)-2-hydroxy-octyl ester 
• 131844-15-0 2-[6-(4-Chloro-phenoxy)-hexyl]-propane-1,2,3-triol 
• 124083-15-4 8-(4-Chloro-phenoxy)-2-methylene-octan-1-ol 

Relevant academic research and scientific papers

Phospholipase A2 inhibitors

There is disclosed a method for the treatment of immunoinflammatory conditions, such as allergy, anaphylaxis, asthma and inflammation in mammals which comprises administering to a mammal so afflicated an effective amount of a compound having the formula:

Phospholipase A2 inhibitors

There is disclosed a method for the treatment of immunoinflammatory conditions, such as allergy, anaphylaxis, asthma and inflammation in mammals which comprises administering to a mammal so afflicted an effective amount of a compound having the formula: S

Phenalkoxyalkyl- and phenoxyalkyl-substituted oxiranecarboxylic acids, their use and medicaments containing them

Phenalkoxyalky- and phenoxyalkyl-substituted oxiranecarboxylic acids of the formula STR1 wherein R1 denotes a hydrogen atom (--H), a halogen atom, a lower alkyl group, a lower alkoxy group, a nitro group or a trifluoromethyl group, R2 has one of the meanings of R1, R3 denotes a hydrogen atom (--H) or a lower alkyl group, Y denotes --O--(CH2)m --, m denotes O or an integer from 1 to 4, and n denotes an integer from 2 to 8, with the proviso that the sum of m and n is an integer from 2 to 8, and the salts of the acids are new compounds. They display a hypoglycaemic action in warm-blooded animals. Processes for the preparation of the new compounds and of the intermediate products required for their preparation are described.