Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C12H20N2O2 |
| Molecular Weight | 224.2994 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
| Stereo Comments | Assumed S configuration based on synthesis from isoleucine |
SHOW SMILES / InChI
SMILES
CC[C@H](C)C1=CN=C(CC(C)C)C(=O)N1O
InChI
InChIKey=IUZCDJYHMMWBBE-VIFPVBQESA-N
InChI=1S/C12H20N2O2/c1-5-9(4)11-7-13-10(6-8(2)3)12(15)14(11)16/h7-9,16H,5-6H2,1-4H3/t9-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Mystery of fermented foods--There are friendly molds too!]. | 2001 |
|
| Taxonomic comparison of three different groups of aflatoxin producers and a new efficient producer of aflatoxin B1, sterigmatocystin and 3-O-methylsterigmatocystin, Aspergillus rambellii sp. nov. | 2005 Jul |
|
| Rapid analysis of fungal cultures and dried figs for secondary metabolites by LC/TOF-MS. | 2008 Jun 9 |
|
| Two novel aflatoxin-producing Aspergillus species from Argentinean peanuts. | 2008 Mar |
|
| 2-(3-Chloro-1,2-dihydro-pyrazin-2-yl-idene)malononitrile. | 2009 Feb 28 |
|
| Polyphasic taxonomy of the heat resistant ascomycete genus Byssochlamys and its Paecilomyces anamorphs. | 2009 Jun |
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41YKP41T0A
Created by
admin on Sat Dec 16 09:59:05 GMT 2023 , Edited by admin on Sat Dec 16 09:59:05 GMT 2023
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22939
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m2101
Created by
admin on Sat Dec 16 09:59:05 GMT 2023 , Edited by admin on Sat Dec 16 09:59:05 GMT 2023
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DTXSID10871687
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490-02-8
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28125533
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admin on Sat Dec 16 09:59:05 GMT 2023 , Edited by admin on Sat Dec 16 09:59:05 GMT 2023
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Aspergillic acid
Created by
admin on Sat Dec 16 09:59:05 GMT 2023 , Edited by admin on Sat Dec 16 09:59:05 GMT 2023
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ACTIVE MOIETY
