Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H6O2S |
| Molecular Weight | 118.154 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=S1(=O)CC=CC1
InChI
InChIKey=MBDNRNMVTZADMQ-UHFFFAOYSA-N
InChI=1S/C4H6O2S/c5-7(6)3-1-2-4-7/h1-2H,3-4H2
| Molecular Formula | C4H6O2S |
| Molecular Weight | 118.154 |
| 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 |
|---|---|---|
| [Creation of functional organic compounds and their applications]. | 2002 Feb |
|
| The hetero-Diels-Alder addition of sulfur dioxide to 1-fluorobuta-1,3-dienes: the sofa conformations preferred by 6-fluorosultines (6-fluoro-3,6-dihydro-1,2-oxathiin-2-oxides) enjoy enthalpic and conformational Anomeric effects. | 2002 Mar 15 |
|
| Ring inversion, structural stability and vibrational assignments of sulfolane c-C4H8SO2 and 3-sulfolene c-C4H6SO2. | 2008 Oct |
|
| [Purification of sulfolene and its UV-Vis and FTIR spectral analysis]. | 2009 Feb |
|
| The Diels-Alder cycloaddition reaction in the functionalization of carbon nanofibers. | 2009 Oct |
|
| Synthesis of oxa-bridged derivatives from Diels-Alder bis-adducts of butadiene and 1,2,3,4-tetrahalo-5,5-dimethoxycyclopentadiene. | 2010 Jun 14 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:16:13 GMT 2023
by
admin
on
Sat Dec 16 02:16:13 GMT 2023
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| Record UNII |
Z6003L44MN
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| Record Status |
Validated (UNII)
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| Record Version |
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77-79-2
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6498
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DTXSID6021294
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56373
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m10356
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201-059-7
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2,5-Dihydrothiophene 1,1-dioxide
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Z6003L44MN
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48532
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2903
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