187264-97-7

Basic information

• Product Name: (5S)-5-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)dihydrofuran-2(3H)-one
• Synonyms: (5S)-5-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)dihydrofuran-2(3H)-one
• CAS NO: 187264-97-7
• Molecular Weight: 200.235
• Mol File: 187264-97-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (5S)-5-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)dihydrofuran-2(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5S)-5-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)dihydrofuran-2(3H)-one(187264-97-7)
• EPA Substance Registry System: (5S)-5-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)dihydrofuran-2(3H)-one(187264-97-7)

Safety Data

• Hazardous Substances Data: 187264-97-7(Hazardous Substances Data)

Usage

General Description

The chemical "(5S)-5-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)dihydrofuran-2(3H)-one" is a compound with a molecular formula of C10H16O4. It is a dihydrofuran-2(3H)-one derivative with a (5S) configuration, and it contains a tetrahydro-2H-pyran-2-yl group attached to the oxygen atom. This chemical is likely to have applications in organic synthesis, medicinal chemistry, and pharmaceuticals due to its unique structure and potential reactivity. Its properties and potential uses make it a compound of interest for further study and exploration in various fields of chemistry and biochemistry.

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 32780-06-6 (5S)-5-(hydroxymethyl)-2-oxo-tetrahydrofuran 

Downstream Products

• 1221442-84-7 N-(4-(7-(((5R)-4-oxaspiro[2.4]heptane-5-yl)methoxy)quinolin-4-yloxy)-3-fluorophenyl)-2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazole-4-carboxamide 
• 1221443-03-3 N'-(4-(7-(((5R)-4-oxaspiro[2.4]heptane-5-yl)methoxy)quinolin-4-yloxy)-3-fluorophenyl)-N-phenylcyclopropane-1,1-dicarboxamide 
• 36326-34-8 (S)-(5,5-dimethyltetrahydrofuran-2-yl)methanol 
• 133328-94-6 (4S,5S)-5-Benzyloxy-4-propyl-tetrahydro-pyran-2-one 
• 133328-93-5 (4R,5S)-5-Benzyloxy-4-propyl-tetrahydro-pyran-2-one 
• 133328-95-7 (4S,5S)-5-Benzyloxy-4-methyl-tetrahydro-pyran-2-one 
• 133328-95-7 (4R,5S)-5-Benzyloxy-4-methyl-tetrahydro-pyran-2-one 
• 133328-96-8 (4R,5S)-5-Benzyloxy-4-butyl-tetrahydro-pyran-2-one 
• 133328-91-3 (S)-5-Benzyloxy-tetrahydro-pyran-2-one 
• 119770-85-3 (S)-5-Benzyloxy-5,6-dihydro-pyran-2-one 
• 334947-47-6 (2S,5E)-7-acetoxy-1-tert-butyldiphenylsiloxy-5-hepten-1-ol 

Relevant articles and documents

Ring-opened 4-hydroxy-δ-valerolactone subunit as a key structural fragment of polyesters that degrade without acid formation

Random copolymers of ?-caprolactone with O-benzyl-protected 4-hydroxy- or 2,4-dihydroxy-δ-valerolactone after hydrogenation form γ-hydroxy functionalized polyesters that degrade via the cyclization to γ-butyrolactone fragments without carboxylic acid formation.

NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS

Disclosed herein are cannabinoid receptor ligands of formula (I) wherein A1, A5, Rx, X4, and z are as defined in the specification. Compositions comprising such compounds, and methods for treating conditions and disorders using such compounds and compositions are also disclosed.

Synthesis of 2,5-disubstituted tetrahydrofurans catalyzed by palladium(0)

A stereoselective cyclization of an allylic ester to 2,5-disubstituted tetrahydrofurans catalyzed by palladium(0) is demonstrated. In this cyclization, acetoxy heptenol (6a) having a free hydroxy group prefered trans isomer to cis isomer. By the use of the protected acetoxy heptenol (6b), the cis selectivity was observed. The stereoselectivity was enhanced by the use of DPPIO ligand.