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
SMILES
O=CC1=COC=C1
InChI
InChIKey=AZVSIHIBYRHSLB-UHFFFAOYSA-N
InChI=1S/C5H4O2/c6-3-5-1-2-7-4-5/h1-4H
| 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
| Title | Date | PubMed |
|---|---|---|
| Photoisomerization and photochemistry of matrix-isolated 3-furaldehyde. | 2010-12-02 |
|
| 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. | 2010-05-26 |
|
| A direct RP-HPLC method for the determination of furanic aldehydes and acids in honey. | 2009-04-15 |
|
| Total synthesis of 20-norsalvinorin A. 1. Preparation of a key intermediate. | 2009-03-20 |
|
| Synthesis of heteroaryl imines: theoretical and experimental approach to the determination of the configuration of C=N double bond. | 2006-09-15 |
|
| Synthesis of new lipophilic ipomeanol analogues and their cytotoxic activities. | 2005-01 |
|
| [Studies on the chemical constituents of the volatiles of Clerodendron bungei]. | 2004-02 |
|
| Synthesis of (+)-manoalide via a copper(I)-mediated 1,2-metalate rearrangement. | 2003-05-16 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:49:17 GMT 2025
by
admin
on
Mon Mar 31 19:49:17 GMT 2025
|
| Record UNII |
POB632X444
|
| Record Status |
Validated (UNII)
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| Record Version |
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POB632X444
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498-60-2
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admin on Mon Mar 31 19:49:17 GMT 2025 , Edited by admin on Mon Mar 31 19:49:17 GMT 2025
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