Details
Stereochemistry | ACHIRAL |
Molecular Formula | C3H6S2 |
Molecular Weight | 106.21 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CSCS1
InChI
InChIKey=IMLSAISZLJGWPP-UHFFFAOYSA-N
InChI=1S/C3H6S2/c1-2-5-3-4-1/h1-3H2
Molecular Formula | C3H6S2 |
Molecular Weight | 106.21 |
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 |
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Alpha-keto amide peptides: a synthetic strategy to resin-bound peptide isosteres for protease inhibitor screening on solid support. | 2004 Mar-Apr |
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Heteroatom-substituted expanded radialenes: one-pot synthesis and characterization of expanded 1,3-dithiolane[n]radialenes. | 2005 Aug 19 |
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gem-Difluorination of 2,2-diaryl-1,3-dithiolanes by Selectfluor and pyridinium polyhydrogen fluoride. | 2005 Feb 7 |
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Reaction of the acetals with TESOTf-base combination; speculation of the intermediates and efficient mixed acetal formation. | 2006 May 3 |
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Intramolecular thia-anti-Michael addition of a sulfur anion to enones: a regiospecific approach to multisubstituted thiophene derivatives. | 2006 Oct 13 |
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Combined 3D QSAR and molecular docking studies to reveal novel cannabinoid ligands with optimum binding activity. | 2007 Dec 15 |
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A new, stereoselective, ring-forming reaction of 1,2-ethanedithiol with N-acylated indoles. | 2007 Nov 9 |
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Synthesis, DNA intercalation and 3D QSAR analysis of cis-2,4,5-trisubstituted-1,3-dithiolanes as a novel class of antitumor agents. | 2009 Aug 15 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:45:44 GMT 2023
by
admin
on
Fri Dec 15 17:45:44 GMT 2023
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Record UNII |
341G58G6YL
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Record Status |
Validated (UNII)
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Record Version |
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341G58G6YL
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4829-04-3
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193357
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C012948
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38335
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DTXSID90197473
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DITHIOLANE
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38079
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20970
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