13417-49-7

Usage

Uses

Used in Chemical Synthesis:
5,6-Dihydro-2H-pyran-3-carbaldehyde is used as a synthetic intermediate for the production of various chemical compounds. Its unique structure allows it to be a versatile building block in the synthesis of a wide range of organic molecules.
Used in Pharmaceutical Industry:
5,6-Dihydro-2H-pyran-3-carbaldehyde is used as a key intermediate in the synthesis of pharmaceutical compounds. Its ability to form stable derivatives and its reactivity make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
5,6-Dihydro-2H-pyran-3-carbaldehyde is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique properties enable the development of effective and environmentally friendly products.
Used in Polymer Industry:
5,6-Dihydro-2H-pyran-3-carbaldehyde is used as a monomer in the production of polymers. Its ability to form stable polymers with desirable properties makes it a valuable component in the development of new materials.
Used in Flavor and Fragrance Industry:
5,6-Dihydro-2H-pyran-3-carbaldehyde is used as a building block in the synthesis of flavor and fragrance compounds. Its unique structure allows for the creation of novel and complex scents and tastes.

InChI:InChI=1/C6H8O2/c7-4-6-2-1-3-8-5-6/h2,4H,1,3,5H2

Upstream product

• 107-02-8 acrolein 
• 79-00-5 1,1,2-trichloroethane 
• 71-55-6 1,1,1-trichloroethane 

Downstream Products

• 86129-89-7 N,3,3-Triphenyl-4-(5,6-dihydro-2H-pyran-3-yl)-2-azetidinone 
• 106273-64-7 3,5-dinitro-benzoic acid-(5,6-dihydro-2H-pyran-3-ylmethyl ester) 
• 1376827-64-3 diphenyl (5,6-dihydro-2H-pyran-3-carbonyl)phosphoramidate 
• 100313-48-2 5,6-dihydro-2H-pyran-3-carboxylic acid 
• 77342-93-9 tetrahydro-pyran-3-carbaldehyde 
• 14774-35-7 (S)-tetrahydropyran-3-yl-carboxaldehyde 
• 14774-36-8 rac-(tetrahydro-2H-pyran-3-yl)methanol 
• 107920-46-7 benzoyloxy-(5,6-dihydro-2H-pyran-3-yl)-acetonitrile 
• 1050493-77-0 2-(tetrahydro-2H-pyran-3-yl)ethanol 
• 23917-19-3 4-(2-hydroxy-3,5-dimethyl-phenyl)-octahydro-pyrano[4,3-d]pyrimidin-2-one 
• 23903-35-7 4-(4-hydroxy-3,5-dimethyl-phenyl)-octahydro-pyrano[4,3-d]pyrimidin-2-one 
• 7179-99-9 (tetrahydro-2H-pyran-3-yl)methanamine 
• 133609-82-2 5,6-Dihydro-2H-pyran-3-carbonsaeure-(α-cyano-3'-phenoxy)-benzylester 

Relevant academic research and scientific papers

COMPOUNDS AND METHODS OF TREATING OCULAR DISORDERS

A method of treating an ocular disorder in a subject associated with increased all-trans-retinal in an ocular tissue includes administering to the subject a therapeutically effective amount of a primary amine compound of formula (I); and pharmaceutically acceptable salts thereof.

Iridium-catalyzed enantioselective hydrogenation of unsaturated heterocyclic acids

Spiral binding: A highly enantioselective hydrogenation of unsaturated heterocyclic acids has been developed by using chiral iridium/spirophosphino oxazoline catalysts (see scheme; BArF-=tetrakis[3,5- bis(trifluoromethyl)phenyl]borate, Boc=tert-butoxycarbonyl). This reaction provided an efficient method for the preparation of optically active heterocyclic acids with excellent enantioselectivities. Copyright

The enantioselective hydrogenation of 5,6-dihydro-2H-pyran-3-carboxylic acid over a cinchona alkaloid-modified palladium catalyst: Asymmetric synthesis of a cockroach attractant

A novel application of a cinchona-modified supported Pd catalyst is presented. The key step in the asymmetric synthesis of the cockroach attractant methyl (+)-tetrahydro-2H-pyran-3-carboxylate was the enantioselective hydrogenation of 5,6-dihydro-2H-pyran

PURINE DERIVATIVES AS IMMUNOMODULATORS

The present invention includes novel compounds useful in the treatment of various disorders in particular infectious diseases, cancer, and allergic diseases and other inflammatory conditions for example allergic rhinitis and asthma, and as vaccine adjuvants

Derivatives of 5,6-Dihydro-2H-pyran-3-carboxylic acid

Some derivatives of 5,6-dihydro-2H-pyran-3-carboxaldehyde (7) and of its oxidation product 5,6-dihydro-2H-pyran-3-carboxylic acid (8) have been prepared.The aldehyde derivatives as well as the amides and esters of 8 have been tested in an insecticidal/fun

Preparation of 3-formyl-5,6-dihydro-2H-pyran

3-Formyl-5,6-dihydro-2H-pyran is prepared by conversion of acrolein in the presence of water, acids and halohydrocarbons of 1 to 6 carbon atoms and 1 to 6 halogen atoms as solvents at from 60° to 150° C. The 3-formyl-5,6-dihydro-2H-pyran obtained by the n