Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H12O2 |
| Molecular Weight | 128.169 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC(=O)OCC=C
InChI
InChIKey=RMZIOVJHUJAAEY-UHFFFAOYSA-N
InChI=1S/C7H12O2/c1-3-5-7(8)9-6-4-2/h4H,2-3,5-6H2,1H3
| Molecular Formula | C7H12O2 |
| Molecular Weight | 128.169 |
| 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 |
|---|---|---|
| Induction of histone acetylation and inhibition of growth of mouse erythroleukemia cells by S-allylmercaptocysteine. | 2002 |
|
| Development of a functional backbone cyclic mimetic of the HIV-1 Tat arginine-rich motif. | 2000-08-04 |
|
| Allyl compounds selectively killed human immunodeficiency virus (type 1)-infected cells. | 1993-07-30 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:56:18 GMT 2025
by
admin
on
Mon Mar 31 18:56:18 GMT 2025
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| Record UNII |
DH3T4NN0KO
|
| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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JECFA EVALUATION |
ALLYL BUTYRATE
Created by
admin on Mon Mar 31 18:56:18 GMT 2025 , Edited by admin on Mon Mar 31 18:56:18 GMT 2025
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CFR |
21 CFR 172.515
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admin on Mon Mar 31 18:56:18 GMT 2025 , Edited by admin on Mon Mar 31 18:56:18 GMT 2025
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2051-78-7
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16324
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1084215
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332
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DTXSID0047666
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DH3T4NN0KO
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218-129-8
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18600
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