3680-96-4

Basic information

• Product Name: 5-MORPHOLIN-4-YL-FURAN-2-CARBALDEHYDE
• Synonyms: CHEMBRDG-BB 4300152;5-MORPHOLIN-4-YL-FURAN-2-CARBALDEHYDE;5-MORPHOLIN-4-YL-2-FURALDEHYDE;5-morpholinofuran-2-carbaldehyde;5-morpholin-4-yl-2-furaldehyde(SALTDATA: FREE)
• CAS NO: 3680-96-4
• Molecular Formula: C₉H₁₁NO₃
• Molecular Weight: 181.19
• Mol File: 3680-96-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 354.5 °C at 760 mmHg
• Flash Point: 168.2 °C
• Appearance: /
• Density: 1.23 g/cm³
• Vapor Pressure: 3.34E-05mmHg at 25°C
• Refractive Index: 1.553
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 5-MORPHOLIN-4-YL-FURAN-2-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-MORPHOLIN-4-YL-FURAN-2-CARBALDEHYDE(3680-96-4)
• EPA Substance Registry System: 5-MORPHOLIN-4-YL-FURAN-2-CARBALDEHYDE(3680-96-4)

Safety Data

• Hazardous Substances Data: 3680-96-4(Hazardous Substances Data)

Usage

General Description

5-Morpholin-4-yl-furan-2-carbaldehyde is a chemical compound with the molecular formula C11H13NO3. It is a furan derivative with a morpholine ring and a aldehyde functional group. 5-MORPHOLIN-4-YL-FURAN-2-CARBALDEHYDE has potential pharmacological activity and has been studied for its use in the development of new drugs and pharmaceuticals. It may also have applications in organic synthesis and as a building block for the preparation of other compounds. Its chemical structure and properties make it a promising candidate for further research and potential use in various fields, including medicine and chemical synthesis.

InChI:InChI=1/C9H11NO3/c11-7-8-1-2-9(13-8)10-3-5-12-6-4-10/h1-2,7H,3-6H2

Upstream product

• 110-91-8 morpholine 
• 2689-65-8 5-iodofuran-2-carbaldehyde 
• 1899-24-7 5-bromo-2-furancarboxaldehyde 
• 3680-95-3 [1-(5-Iodo-furan-2-yl)-meth-(E)-ylidene]-phenyl-amine 
• 31795-44-5 5-formyl-2-furansulfonic acid sodium salt 
• 5207-56-7 5-N-morpholylfurfurylidene-N-morpholidium iodide 

Downstream Products

• 1017832-06-2 C₁₉H₁₆N₂O₄ 
• 444668-27-3 C₁₆H₁₈N₂O₂ 
• 1225043-38-8 ethyl 2-(4-methoxyphenyl)-5-morpholino-3-oxo-2,3-dihydro-1H-isoindole-4-carboxylate 
• 1146445-63-7 (3R,9bS)-ethyl 2,3,5,9b-tetrahydro-7-morpholino-5-oxo-3-phenyloxazolo[2,3-a]isoindole-6-carboxylate 
• 1146445-65-9 (3S,9bR)-ethyl 3-benzyl-2,3,5,9b-tetrahydro-7-morpholino-5-oxooxazolo[2,3-a]isoindole-6-carboxylate 
• 1146445-69-3 (2R,3S,9br)-ethyl 2,3,5,9b-tetrahydro-3-methyl-7-morpholino-5-oxo-2-phenyloxazolo[2,3-a]isoindole-6-carboxylate 
• 1144506-68-2 1-(5-morpholinofur-2-yl)-1-phenylmethanol 
• 84966-23-4 (1-Hydroxycyclohexyl)-N-(5-morpholinofurfuryliden)methanamin-N-oxid 
• 54478-76-1 4-[5-(4-nitro-phenylazo)-furan-2-yl]-morpholine 

Relevant articles and documents

A facile preparation of trisubstituted amino-furan and -thiophene derivatives

β-Alkylation of amino-furan and -thiophene heterocycles is described through metal-, acid- and base-free carbon-carbon bond formation. The ability of both heterocycles to undergo selective β-alkylation is compared by mean of experimental and theoretical data. The presence of chiral amine substituents induced the diastereoselective generation of the newly formed additional stereocenter.

BCRP/ABCG2 INHIBITOR

The present invention is directed to a breast cancer resistance protein (BCRP/ABCG2) inhibitor. The BCRP inhibitor contains, as an active ingredient, an acrylonitrile derivative represented by formula (1): wherein one of R1 and R2 re

Ring-Chain Isomerism of N-(2-Hydroxyalkyl)nitrones, III. Nitrones of 2-Furancarbaldehydes

The ring-chain isomerism of N-(2-hydroxyalkyl)nitrones 3, obtained from 2-furancarbaldehyde and its 5-dialkylamino and 5-nitro derivatives, is studied by acylation of 3 with diphenylborinic acid, carboxylic acids, and isocyanates.Dependent on the kind of