96557-31-2

Usage

Colorless liquid

This refers to the physical appearance of the compound, which is a clear and transparent liquid.

Sweet and floral odor

This describes the smell of the compound, which is described as sweet and reminiscent of flowers.

Flavoring agent in the food industry

This refers to the use of the compound as an additive in food products to impart a specific taste or aroma.

Fragrance in the perfume industry

This refers to the use of the compound as an ingredient in perfumes and other fragrances to provide a desired scent.

Production of pharmaceuticals

This refers to the use of the compound as a starting material or intermediate in the synthesis of drugs.

Intermediate in organic synthesis

This refers to the use of the compound as a reactant in chemical reactions to produce other compounds.

Biological and pharmacological activities

This refers to the study of the compound's potential effects on living organisms and its therapeutic properties.

Antimicrobial and antifungal properties

This refers to the compound's ability to inhibit the growth of microorganisms and fungi.

Harmful if ingested, inhaled, or absorbed through the skin

This is a warning about the potential hazards of handling the compound, which can cause harm to the body if it is swallowed, breathed in, or comes into contact with the skin.

Upstream product

• 2591-86-8 N-Formylpiperidine 
• 96557-36-7 2-(2-Bromphenyl)-acetaldehydethylenacetal 
• 764-48-7 ethyleneglycol vinyl ether 
• 6630-33-7 ortho-bromobenzaldehyde 
• 96557-30-1 2-bromophenylacetaldehyde 
• 1074-16-4 2-bromophenylethyl alcohol 

Downstream Products

• 96557-32-3 dimethyl 2,6-dimethyl-4-<2-((2-(1,3-dioxolanyl))methyl)phenyl>-1,4-dihydropyridine-2,6-dicarboxylate 

Relevant academic research and scientific papers

Direct synthesis of protected arylacetaldehydes by tetrakis(phosphane)- palladium-catalyzed arylation of ethyleneglycol vinyl ether

A range of aryl bromides undergo Heck reaction with ethylene glycol vinyl ether, in the presence of [PdCl(C3H5)]2/ cis,cis,cis-1,2,3,4-tetrakis[(diphenylphosphanyl)methyl]cyclopentane as catalyst, to give regioselectively protected arylacetaldehydes in good yields. The β-arylation products were obtained in with 93-100 % selectivity with electron-poor aryl bromides or heteroaryl bromides. Furthermore, this catalyst can be used at low loading, even for reactions with sterically hindered aryl bromides. The aryl vinyl ether intermediates undergo subsequent ketalisation to give the corresponding 2-benzyl-1,3-dioxolane derivatives. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

Direct synthesis of protected arylacetaldehydes by palladium- tetraphosphine-catalyzed arylation of ethyleneglycol vinylether

Through the use of [PdCl(C3H5)]2/cis,cis, cis-1,2,3,4-tetrakis(diphenylphosphinomethyl) cyclopentane as a catalyst, a range of aryl bromides undergo Heck reaction with ethyleneglycol vinylether to give regioselectively protected arylacetaldehydes in good yields. The β-arylation products were obtained in the range 93-98% selectivity with electron-poor aryl bromides. Furthermore, this catalyst can be used at low loading, even for reactions of sterically hindered aryl bromides. The arylvinyl ethers intermediates undergo subsequent ketalization to give the corresponding 2-benzyl-1,3-dioxolane derivatives.

Iminium Ion Mediated Cyclizations of 4-Aryl-1,4-dihydropyridines. Bridging with Acetals, Carbonyls, and Thiocarbonyls

The preparation of new aldehyde and acetal derivatives of 4-aryl-1,4-dihydropyridines has been carried out.Treatment of these compounds under acid conditions affords novel caged molecules derived from sequential intramolecular addition reactions.This proc