Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H10O2 |
| Molecular Weight | 150.1745 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)OC1=CC=C(C)C=C1
InChI
InChIKey=CDJJKTLOZJAGIZ-UHFFFAOYSA-N
InChI=1S/C9H10O2/c1-7-3-5-9(6-4-7)11-8(2)10/h3-6H,1-2H3
| Molecular Formula | C9H10O2 |
| Molecular Weight | 150.1745 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionCurator's Comment: The description was created based on several sources, including
http://pubs.acs.org/doi/abs/10.1021/ja00502a074?journalCode=jacsat
Curator's Comment: The description was created based on several sources, including
http://pubs.acs.org/doi/abs/10.1021/ja00502a074?journalCode=jacsat
p-Cresyl Acetate is used in formulating perfumeries, fragrances, and disinfectants. p-Cresyl acetate is used as the starting material for the synthesis of 2-acetyl-4-methylphenol.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Structure elucidation and inhibitory effects of self-assembled organotin(IV) esters of p-tolyl acetic acid on bacterial, fungal, brine shrimp, and potato tumor cells. | 2010-04 |
|
| Multienzyme catalysis in microfluidic biochips. | 2003-07-05 |
|
| Synthesis and antimycobacterial activity of pyrazine and quinoxaline derivatives. | 2002-12-05 |
| Substance Class |
Chemical
Created
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admin
on
Edited
Mon Mar 31 18:17:00 GMT 2025
by
admin
on
Mon Mar 31 18:17:00 GMT 2025
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| Record UNII |
42I5PWW20C
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| Record Status |
Validated (UNII)
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CFR |
21 CFR 172.515
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JECFA EVALUATION |
P-TOLYL ACETATE
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140-39-6
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C007147
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43244
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578
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205-413-1
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65594
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42I5PWW20C
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