86266-57-1

Usage

Tetrahydropyran ring

A cyclic structure composed of five carbon atoms and one oxygen atom, which provides the compound with a specific spatial arrangement and stability.

Acetaldehyde group

A functional group consisting of a carbonyl group (C=O) bonded to two hydrogen atoms, which gives the compound its characteristic aldehyde properties and reactivity.

Colorless liquid

The compound lacks color in its pure form, which is a physical property that can be observed without any chemical analysis.

Fruity odor

The compound has a distinct smell similar to fruits, which is a sensory property that can be detected by smell.

Flavoring agent

The compound is used to add or enhance flavors in food and beverages, which is an application of its functional properties.

Synthesis of pharmaceuticals

The compound is used as an intermediate in the production of various drugs, which highlights its importance in the pharmaceutical industry.

Synthesis of other organic compounds

The compound can be used as a building block to create other organic molecules, which is a testament to its versatility in organic synthesis.

Low acute toxicity

The compound has a low level of toxicity when ingested or exposed to in the short term, which is a measure of its relative safety in controlled environments.

Prolonged exposure can cause irritation

The compound can cause skin, eye, and respiratory irritation if exposure is prolonged, which is a potential health hazard to consider when handling the compound.

Handling and storage precautions

The compound should be handled and stored with care to avoid any adverse health effects, which is a safety measure to ensure proper use and disposal of the compound.

Upstream product

• 142-68-7 TETRAHYDROPYRANE 
• 85684-59-9 percarbonate de O,O-t-butyle et O-vinyle 
• 38786-79-7 2-(tetrahydropyran-2-yl)ethanol 
• 38786-78-6 (+/-)-ethyl tetrahydro-2H-pyran-2-acetate 
• 1050494-60-4 2-[(E/Z)-2-methoxyethenyl]tetrahydro-2H-pyran 
• 89794-62-7 (E)-hept-2-ene-1,7-diol 
• 96251-91-1 ethyl cis/trans-7-hydroxy-2-heptenoate 
• 181273-30-3 (E)-7-(Tetrahydro-pyran-2-yloxy)-hept-2-enoic acid ethyl ester 

Downstream Products

• 860010-76-0 1-tetrahydro-2H-2-pyranylmethyl allyl-2-benzyloxy acetate 
• 38786-79-7 2-(tetrahydropyran-2-yl)ethanol 
• 1312019-05-8 1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-2-yl)-ethanol 
• 1312016-92-4 2-[1(R)-(4-methanesulfonyl-phenyl)-2-(tetrahydro-pyran-2(S)-yl)-ethyl-]-1H-pyrrolo[2,3-b]pyridine 
• 1312021-17-2 2-[1(S)-(4-methanesulfonyl-phenyl)-2-(tetrahydro-pyran-2(S)-yl)-ethyl-]-1H-pyrrolo[2,3-b]pyridine 
• 1312019-09-2 toluene-4-sulfonic acid 1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-yl)-vinyl ester 
• 1312019-08-1 1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-2(S)-yl)-ethanone 
• 1312019-07-0 1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-2(R)-yl)-ethanone 
• 1312019-11-6 2-[1-(4-methanesulfonyl-phenyl)-2-(tetrahydro-pyran-2-yl)-vinyl]-1H-pyrrolo[2,3-b]pyridine 
• 1312019-10-5 1-benzenesulfonyl-2-[1-(4-methanesulfonyl-phenyl)-2-(tetrahydro-pyran-2-yl)-vinyl]-1H-pyrrolo[2,3-b]pyridine 
• 1312019-06-9 1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-2-yl)-ethanone 

Relevant academic research and scientific papers

AZAINDOLE GLUCOKINASE ACTIVATORS

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of metabolic diseases and disorders such as, for example, type II diabetes mellitus.

Organocatalytic synthesis of an alkyltetrahydropyran

The first synthesis of an alkyltetrahydropyran using a diarylprolinol organocatalyst is described. Georg Thieme Verlag Stuttgart.

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

A novel synthesis of the north west portion of Lasonolide A - An anticancer macrolide using Claisen rearrangement

A simplified analogue of Lasonolide A (C23-C35 side chain) was synthesized using Fujisawa's stereoselective variant of the Ireland Claisen ester rearrangement.

Obtention d'aldehydes γ-fonctionnels au cours de la thermolyse du percarbonate de O,O-t-butyle et O-vinyle en solution

Owing to its peroxyester group, O,O-tert-butyl and O-vinyle peroxycarbonate may act as a free radical initiator in solution, but also, due to the presence of the vinylic insaturation, as a substrate for free radical addition reactions. - In such solvents as cumene which give free radicals unable to add to the double bond, the peroxycarbonate merely behaves as a vinyloxy radicals generator.It is thus possible to observe these radicals reacting either as formylmethyl radicals or as acetyl radicals. - In solvents such as cyclohexane which give free radicals able to add to the double bond, the reaction results in the substitution of formylmethyl groups to labile hydrogens of the solvent. - By applying the reaction to such compounds as ketones, ethers, acids and their derivatives, we could obtain γ-functional aldehydes (γ-ketoaldehydes, γ-oxaaldehydes and derivatives of succinaldehydic acids).These products are often difficult to prepare by other routes and until now only some of them have been described.