Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H6O4S |
| Molecular Weight | 150.153 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CSCC(O)=O
InChI
InChIKey=UVZICZIVKIMRNE-UHFFFAOYSA-N
InChI=1S/C4H6O4S/c5-3(6)1-9-2-4(7)8/h1-2H2,(H,5,6)(H,7,8)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of new chiral sulfinyldiacetic acid derivatives and attempt at chemoselective asymmetric Pummerer reaction. | 2002 Apr |
|
| Voltammetric determination of thiodiglycolic acid in urine. | 2003 Jan |
|
| Dialkyl 3,3'-thiodipropionate and dialkyl 2,2'-thiodiacetate antioxidants by lipase-catalyzed esterification and transesterification. | 2006 Apr 19 |
Patents
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Code | English |
| Code System | Code | Type | Description | ||
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C010518
Created by
admin on Sat Dec 16 20:01:05 GMT 2023 , Edited by admin on Sat Dec 16 20:01:05 GMT 2023
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204-663-9
Created by
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35012
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m10754
Created by
admin on Sat Dec 16 20:01:05 GMT 2023 , Edited by admin on Sat Dec 16 20:01:05 GMT 2023
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DTXSID1051432
Created by
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2707
Created by
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483M3RG5GW
Created by
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31277
Created by
admin on Sat Dec 16 20:01:05 GMT 2023 , Edited by admin on Sat Dec 16 20:01:05 GMT 2023
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28743
Created by
admin on Sat Dec 16 20:01:05 GMT 2023 , Edited by admin on Sat Dec 16 20:01:05 GMT 2023
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123-93-3
Created by
admin on Sat Dec 16 20:01:05 GMT 2023 , Edited by admin on Sat Dec 16 20:01:05 GMT 2023
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PRIMARY |
PARENT (METABOLITE)
SUBSTANCE RECORD
