Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H7ClO2 |
| Molecular Weight | 170.593 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1)C(Cl)=O
InChI
InChIKey=MXMOTZIXVICDSD-UHFFFAOYSA-N
InChI=1S/C8H7ClO2/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3
| Molecular Formula | C8H7ClO2 |
| Molecular Weight | 170.593 |
| 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 |
|---|---|---|
| N'-(4-Methoxy-benzo-yl)pyridine-2-carbohydrazide. | 2010-04-24 |
|
| Generating a generation of proteasome inhibitors: from microbial fermentation to total synthesis of salinosporamide a (marizomib) and other salinosporamides. | 2010-03-25 |
|
| 3-(4-Methoxy-phen-yl)isochroman-1-one. | 2008-10-15 |
|
| Synthesis of 6-O-methyl ether of Scorzocreticin and Scorzocreticoside I, metabolites from Sorzonera cretica. | 2006-07-26 |
|
| Solvent polarity and organic reactivity in mixed solvents: evidence using a reactive molecular probe to assess the role of preferential solvation in aqueous alcohols. | 2005-03-04 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:19:03 GMT 2025
by
admin
on
Mon Mar 31 21:19:03 GMT 2025
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| Record UNII |
TV6DMQ9451
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| Record Status |
Validated (UNII)
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| Record Version |
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