Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8O2 |
| Molecular Weight | 136.1479 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C1=CC=CC(O)=C1
InChI
InChIKey=LUJMEECXHPYQOF-UHFFFAOYSA-N
InChI=1S/C8H8O2/c1-6(9)7-3-2-4-8(10)5-7/h2-5,10H,1H3
| Molecular Formula | C8H8O2 |
| Molecular Weight | 136.1479 |
| 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 |
|---|---|---|
| Chemoenzymatic synthesis of rivastigmine via dynamic kinetic resolution as a key step. | 2010-05-07 |
|
| (E)-3-(4-Hexyl-oxyphen-yl)-1-(3-hydroxy-phen-yl)prop-2-en-one. | 2009-03-28 |
|
| [Synthesis of S-(+)-rivastigmine hydrogentartrate]. | 2007-02 |
|
| Design and syntheses of novel phthalazin-1(2H)-one derivatives as acetohydroxyacid synthase inhibitors. | 2006-11-29 |
|
| Cyclized geranyl stilbenes from the rhizomes of Helminthostachys zeylanica. | 2003-10 |
|
| Comparative inhibition by substrate analogues 3-methoxy- and 3-hydroxydesaminokynurenine and an improved 3 step purification of recombinant human kynureninase. | 2003-09-24 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:45:37 GMT 2025
by
admin
on
Mon Mar 31 18:45:37 GMT 2025
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| Record UNII |
UV3GO1D90J
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| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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C551129
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2440
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DTXSID5059533
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2560214
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UV3GO1D90J
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3'-Hydroxyacetophenone
Created by
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121-71-1
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UV3GO1D90J
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8487
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204-494-0
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| Related Record | Type | Details | ||
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