Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.1525 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NCC1=CC=C(O)C=C1
InChI
InChIKey=RQJDUEKERVZLLU-UHFFFAOYSA-N
InChI=1S/C7H9NO/c8-5-6-1-3-7(9)4-2-6/h1-4,9H,5,8H2
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.1525 |
| 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 |
|---|---|---|
| (4-Hydroxy-phen-yl)methanaminium 2-(4-sulfanylphen-yl)acetate. | 2009-09-05 |
|
| Synthesis and biological evaluation of aminomethylphenol derivatives as inhibitors of the murine GABA transporters mGAT1-mGAT4. | 2008-11 |
|
| Inhibition of GABA shunt enzymes' activity by 4-hydroxybenzaldehyde derivatives. | 2006-02 |
|
| Inactivation of mitochondrial monoamine oxidase B by methylthio-substituted benzylamines. | 2003-10-01 |
|
| Fragmentation mechanisms of protonated benzylamines. Electrospray ionisation-tandem mass spectrometry study and ab initio molecular orbital calculations. | 2003 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:58:54 GMT 2025
by
admin
on
Mon Mar 31 19:58:54 GMT 2025
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| Record UNII |
7J7F85B7BI
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| Record Status |
Validated (UNII)
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| Record Version |
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696-60-6
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C048829
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DTXSID00219872
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7J7F85B7BI
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