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Details

Stereochemistry ACHIRAL
Molecular Formula C5H4O2
Molecular Weight 96.0841
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-FURANCARBOXALDEHYDE

SMILES

O=CC1=COC=C1

InChI

InChIKey=AZVSIHIBYRHSLB-UHFFFAOYSA-N
InChI=1S/C5H4O2/c6-3-5-1-2-7-4-5/h1-4H

HIDE SMILES / InChI

Molecular Formula C5H4O2
Molecular Weight 96.0841
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis of (+)-manoalide via a copper(I)-mediated 1,2-metalate rearrangement.
2003 May 16
[Studies on the chemical constituents of the volatiles of Clerodendron bungei].
2004 Feb
Synthesis of new lipophilic ipomeanol analogues and their cytotoxic activities.
2005 Jan
Synthesis of heteroaryl imines: theoretical and experimental approach to the determination of the configuration of C=N double bond.
2006 Sep 15
A direct RP-HPLC method for the determination of furanic aldehydes and acids in honey.
2009 Apr 15
Total synthesis of 20-norsalvinorin A. 1. Preparation of a key intermediate.
2009 Mar 20
Photoisomerization and photochemistry of matrix-isolated 3-furaldehyde.
2010 Dec 2
Adsorption and separation of reactive aromatic isomers and generation and stabilization of their radicals within cadmium(II)-triazole metal-organic confined space in a single-crystal-to-single-crystal fashion.
2010 May 26
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:35:19 GMT 2023
Edited
by admin
on Fri Dec 15 19:35:19 GMT 2023
Record UNII
POB632X444
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-FURANCARBOXALDEHYDE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID40198076
Created by admin on Fri Dec 15 19:35:19 GMT 2023 , Edited by admin on Fri Dec 15 19:35:19 GMT 2023
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PUBCHEM
10351
Created by admin on Fri Dec 15 19:35:19 GMT 2023 , Edited by admin on Fri Dec 15 19:35:19 GMT 2023
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FDA UNII
POB632X444
Created by admin on Fri Dec 15 19:35:19 GMT 2023 , Edited by admin on Fri Dec 15 19:35:19 GMT 2023
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CAS
498-60-2
Created by admin on Fri Dec 15 19:35:19 GMT 2023 , Edited by admin on Fri Dec 15 19:35:19 GMT 2023
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