Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H6O3 |
| Molecular Weight | 138.1207 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OOC(=O)C1=CC=CC=C1
InChI
InChIKey=XCRBXWCUXJNEFX-UHFFFAOYSA-N
InChI=1S/C7H6O3/c8-7(10-9)6-4-2-1-3-5-6/h1-5,9H
| Molecular Formula | C7H6O3 |
| Molecular Weight | 138.1207 |
| 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 |
|---|---|---|
| Study of a benzoylperoxy radical in the gas phase: ultraviolet spectrum and C6H5C(O)O2 + HO2 reaction between 295 and 357 K. | 2010-09-30 |
|
| Synthesis and NMR characterization of the methyl esters of eicosapentaenoic acid monoepoxides. | 2009-05 |
|
| Hydrotrioxides rather than cyclic tetraoxides (tetraoxolanes) as the primary reaction intermediates in the low-temperature ozonation of aldehydes. The case of benzaldehyde. | 2009-01-02 |
|
| The loss of carbon dioxide from activated perbenzoate anions in the gas phase: unimolecular rearrangement via epoxidation of the benzene ring. | 2006-10-13 |
|
| Mechanistic studies of Hangman salophen-mediated activation of O-O bonds. | 2006-09-18 |
|
| Self-hydroxylation of perbenzoic acids at a nonheme iron(II) center. | 2005-12-07 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:35:11 GMT 2025
by
admin
on
Mon Mar 31 21:35:11 GMT 2025
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| Record UNII |
C0EZ97V99I
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| Record Status |
Validated (UNII)
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| Record Version |
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523077
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DTXSID10239223
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93-59-4
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C0EZ97V99I
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202-260-2
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m8536
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PRIMARY | Merck Index | ||
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PEROXYBENZOIC ACID
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admin on Mon Mar 31 21:35:11 GMT 2025 , Edited by admin on Mon Mar 31 21:35:11 GMT 2025
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C017611
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