Details
Stereochemistry | RACEMIC |
Molecular Formula | C4H11NOS |
Molecular Weight | 121.201 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)[S+](N)[O-]
InChI
InChIKey=CESUXLKAADQNTB-UHFFFAOYSA-N
InChI=1S/C4H11NOS/c1-4(2,3)7(5)6/h5H2,1-3H3
Molecular Formula | C4H11NOS |
Molecular Weight | 121.201 |
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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N-tert-butanesulfinyl imines: versatile intermediates for the asymmetric synthesis of amines. | 2002 Nov |
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Improved synthesis of tert-butanesulfinamide suitable for large-scale production. | 2003 Apr 17 |
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Practical asymmetric synthesis of alpha-branched 2-piperazinylbenzylamines by 1,2-additions of organometallic reagents to N-tert-butanesulfinyl imines. | 2005 Oct 28 |
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Expedient synthesis of N-methyl tubulysin analogues with high cytotoxicity. | 2008 Jun 20 |
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Highly stereoselective methylene transfers onto butanediacetal-protected chiral non-racemic sulfinyl imines using S-ylide technology. | 2009 Apr 14 |
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Synthesis and applications of tert-butanesulfinamide. | 2010 Jun 9 |
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Discovery of 4-amino-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamides as selective, orally active inhibitors of protein kinase B (Akt). | 2010 Mar 11 |
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The tert-butylsulfinamide lynchpin in transition-metal-mediated multiscaffold library synthesis. | 2010 May 7 |
|
Stereoselective α-aminoallylation of aldehydes with chiral tert-butanesulfinamides and allyl bromides. | 2010 Sep 17 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:02:41 GMT 2023
by
admin
on
Sat Dec 16 10:02:41 GMT 2023
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Record UNII |
42F4K704G0
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Record Status |
Validated (UNII)
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Record Version |
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-
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DTXSID20391967
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146374-27-8
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42F4K704G0
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tert-Butanesulfinamide
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3382465
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admin on Sat Dec 16 10:02:41 GMT 2023 , Edited by admin on Sat Dec 16 10:02:41 GMT 2023
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