Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C4H8O2S |
| Molecular Weight | 120.17 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(CS)C(O)=O
InChI
InChIKey=MHRDCHHESNJQIS-UHFFFAOYSA-N
InChI=1S/C4H8O2S/c1-3(2-7)4(5)6/h3,7H,2H2,1H3,(H,5,6)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| High-performance liquid chromatographic determination of alpha-aminonitrile enantiomers after derivatization with o-phthalaldehyde and chiral thiols. | 2004 Nov 5 |
|
| Bacterial taxa that limit sulfur flux from the ocean. | 2006 Oct 27 |
|
| Comparison of whole body scintigraphy with Tc-99m-methoxyisobutylisonitrile and iodine-131 NA in patients with differentiated thyroid cancer. | 2007 Jan |
Patents
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| Code System | Code | Type | Description | ||
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152910
Created by
admin on Sat Dec 16 02:14:52 GMT 2023 , Edited by admin on Sat Dec 16 02:14:52 GMT 2023
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26473-47-2
Created by
admin on Sat Dec 16 02:14:52 GMT 2023 , Edited by admin on Sat Dec 16 02:14:52 GMT 2023
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247-726-6
Created by
admin on Sat Dec 16 02:14:52 GMT 2023 , Edited by admin on Sat Dec 16 02:14:52 GMT 2023
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DTXSID60865293
Created by
admin on Sat Dec 16 02:14:52 GMT 2023 , Edited by admin on Sat Dec 16 02:14:52 GMT 2023
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V3E4016VAS
Created by
admin on Sat Dec 16 02:14:52 GMT 2023 , Edited by admin on Sat Dec 16 02:14:52 GMT 2023
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PRIMARY |
SUBSTANCE RECORD
