Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.1259 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=CNC1=O
InChI
InChIKey=MVKDNXIKAWKCCS-UHFFFAOYSA-N
InChI=1S/C6H7NO/c1-5-3-2-4-7-6(5)8/h2-4H,1H3,(H,7,8)
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.1259 |
| 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 |
|---|---|---|
| Synthesis of a dA-dT base pair analogue and its effects on DNA-ligand binding. | 2001 Aug |
|
| Minor groove functional groups are critical for the B-form conformation of duplex DNA. | 2001 Jan 30 |
|
| Polaronic semiconductor behavior of long-range charge transfer in DNA oligomers in solution: controlling barriers to long-distance radical cation migration in DNA with thymine analogs. | 2006 |
|
| Origin of methyl torsional barrier in 1-methyl-2(1H)-pyridinimine and 3-methyl-2(1H)-pyridone: II. Ground state. | 2007 Mar 21 |
|
| Spectroscopic studies on methyl torsional behavior in 1-methyl-2(1H)-pyridone, 1-methyl-2(1H)-pyridinimine, and 3-methyl-2(1H)-pyridone. I. Excited state. | 2007 Mar 21 |
|
| Synthesis and phytotoxic activity of new pyridones derived from 4-hydroxy-6-methylpyridin-2(1H)-one. | 2009 Dec 1 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:35:20 GMT 2023
by
admin
on
Fri Dec 15 19:35:20 GMT 2023
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| Record UNII |
VM19FN4HHV
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| Record Status |
Validated (UNII)
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| Record Version |
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