Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H8O2 |
| Molecular Weight | 124.1372 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C1=CC=C(C)O1
InChI
InChIKey=KEFJLCGVTHRGAH-UHFFFAOYSA-N
InChI=1S/C7H8O2/c1-5-3-4-7(9-5)6(2)8/h3-4H,1-2H3
| Molecular Formula | C7H8O2 |
| Molecular Weight | 124.1372 |
| 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 |
|---|---|---|
| Use of phosphonyl carbanions in the synthesis of anti-inflammatory active phosphorus-containing fused heterocycles and relevance phosphonates. | 2010-11 |
|
| Investigation of trypanothione reductase as a drug target in Trypanosoma brucei. | 2009-12 |
|
| Antitubercular constituents from the stem wood of Cinnamomum kotoense. | 2005-09 |
|
| Aging of proteins: immunological detection of a glucose-derived pyrrole formed during maillard reaction in vivo. | 1989-03-05 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:49:16 GMT 2025
by
admin
on
Mon Mar 31 18:49:16 GMT 2025
|
| Record UNII |
IY49408H2O
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
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Download
| Name | Type | Language | ||
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Systematic Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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JECFA EVALUATION |
2-ACETYL-5-METHYLFURAN
Created by
admin on Mon Mar 31 18:49:16 GMT 2025 , Edited by admin on Mon Mar 31 18:49:16 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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14514
Created by
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1193-79-9
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IY49408H2O
Created by
admin on Mon Mar 31 18:49:16 GMT 2025 , Edited by admin on Mon Mar 31 18:49:16 GMT 2025
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80404
Created by
admin on Mon Mar 31 18:49:16 GMT 2025 , Edited by admin on Mon Mar 31 18:49:16 GMT 2025
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562752
Created by
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214-779-1
Created by
admin on Mon Mar 31 18:49:16 GMT 2025 , Edited by admin on Mon Mar 31 18:49:16 GMT 2025
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PRIMARY | |||
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2-Acetyl-5-methylfuran
Created by
admin on Mon Mar 31 18:49:16 GMT 2025 , Edited by admin on Mon Mar 31 18:49:16 GMT 2025
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1495
Created by
admin on Mon Mar 31 18:49:16 GMT 2025 , Edited by admin on Mon Mar 31 18:49:16 GMT 2025
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DTXSID70152409
Created by
admin on Mon Mar 31 18:49:16 GMT 2025 , Edited by admin on Mon Mar 31 18:49:16 GMT 2025
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PRIMARY |