85907-66-0

Usage

Uses

Used in Pharmaceutical Industry:
(Z)-2-(4-CHLOROPHENYL)-3-(DIMETHYLAMINO)-2-PROPENAL is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Research and Development:
In the field of research and development, (Z)-2-(4-CHLOROPHENYL)-3-(DIMETHYLAMINO)-2-PROPENAL serves as a reagent and building block for the creation of complex organic compounds, facilitating advancements in organic synthesis and the discovery of novel chemical entities.
Used in Medicinal Chemistry:
(Z)-2-(4-CHLOROPHENYL)-3-(DIMETHYLAMINO)-2-PROPENAL is employed in medicinal chemistry for its potential to be incorporated into the structures of new drug candidates, contributing to the design and synthesis of molecules with specific biological activities.
Used in Biochemistry:
(Z)-2-(4-CHLOROPHENYL)-3-(DIMETHYLAMINO)-2-PROPENAL also has applications in biochemistry, where it may be used to study enzyme mechanisms, develop new biochemical assays, or understand the interactions between molecules and biological systems.

InChI:InChI=1/C11H12ClNO/c1-13(2)7-10(8-14)9-3-5-11(12)6-4-9/h3-8H,1-2H3/b10-7+

Upstream product

• 1878-66-6 4-chlorophenylacetic Acid 

Downstream Products

• 35982-98-0 5-(4-chlorophenyl)-1,2-dihydro-2-oxo-3-pyridinecarbonitrile 
• 163563-22-2 (Z)-2-(4'-fluorophenyl)-3-N,N-dimethylaminopropenal 
• 85907-67-1 2-(4-Bromophenyl)-3-(dimethylamino)-2-propenal 

Relevant academic research and scientific papers

Dihydropyridazinones, pyridazinones and related compounds as fungicides

This invention relates to substituted dihydropyridazinones, pyridazinones and related compounds, of the formula STR1 wherein A, Q, D and R1 are as defined within, compositions containing these compounds and methods of controlling agricultural and mammalian fungal diseases.

New synthetic routes to 3-, 5-, and 6-aryl-2-chloropyridines

The efficient synthesis of 3-, 5-, and 6-aryl-2-chloropyridines via the facile preparation of 5-(dimethylamino)aryl-substituted pentadienyl nitriles and cyclization with hydrochloric acid is described. This approach allows for the introduction of other electron-withdrawing substituents on the pyridine ring as well as the preparation of the desired unsubstituted arylpyridines. Some differences in the rates of cyclization of the pentadienyl nitriles as well as the yields of chloropyridines were observed that depended on the position and degree of substitution in the aryl substituent. The arylpentadienyl nitriles 5 and 6 could also be converted directly into the corresponding 2-aminopyridines.

Method for inducing tillering utilizing certain pyridine-1-oxides

This invention relates to a method of inducing tillering in cereal plants using certain 5-phenyl-3-pyridinecarboxylate compounds, to certain of the compounds themselves, to a process for preparing these compounds, and to agricultural compositions containing them. The compounds are also useful as intermediates for preparing other of the compounds.

1-Benzoyl-3-(arylphyridyl)urea compounds

The present invention is directed to 1-benzoyl-3-(arylpyridyl)urea compounds useful as insecticides.

Antidiabetic pyrrolecarboxylic acids

Certain pyrrolecarboxylic and pyrroleacetic acid derivatives substituted on the pyrrole ring with thioether groups, acyl groups, phenyl, substituted phenyl, phenoxy, substituted phenoxy, benzyl or halo and optionally substituted on the pyrrole nitrogen with alkyl, and the pharmaceutically acceptable salts thereof, are useful in lowering the blood glucose levels of hyperglycemic animals.

Substituted 6-phenyl-1,2,4-triazolo[4,3-a]pyridines

This disclosure describes novel 6-(substituted-phenyl)-1,2,4-triazolo[4,3-a]pyridines useful as hypotensive agents.

Substituted 3-alkyl-6-phenyl-1,2,4-triazolo-[4,3-a]pyridines

This disclosure describes novel 3-alkyl-6-(substituted-phenyl)-1,2,4-triazolo[4,3-a]pyridines useful as anxiolytic agents.