Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H9NS |
| Molecular Weight | 103.186 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CSCCN1
InChI
InChIKey=BRNULMACUQOKMR-UHFFFAOYSA-N
InChI=1S/C4H9NS/c1-3-6-4-2-5-1/h5H,1-4H2
| Molecular Formula | C4H9NS |
| Molecular Weight | 103.186 |
| 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 |
|---|---|---|
| Natural abundance nitrogen-15 nuclear magnetic resonance spectral studies on selected donors. | 2002 Oct |
|
| New antibacterial tetrahydro-4(2H)-thiopyran and thiomorpholine S-oxide and S,S-dioxide phenyloxazolidinones. | 2003 Dec 1 |
|
| Reactions of sulphur mustard on impregnated carbons. | 2004 Dec 31 |
|
| Antimycobacterial compounds. New pyrrole derivatives of BM212. | 2004 Mar 15 |
|
| Fluorescence-based nitric oxide detection by ruthenium porphyrin fluorophore complexes. | 2004 Oct 4 |
|
| Structure of radical cations of saturated heterocyclic compounds with two heteroatoms as studied by electron paramagnetic resonance, electron-nuclear double resonance, and density functional theory calculations. | 2005 Jul 21 |
|
| Kinetics of degradation of sulphur mustard on impregnated carbons. | 2005 May 20 |
|
| Selective phosphorescence chemosensor for homocysteine based on an iridium(III) complex. | 2007 Dec 24 |
|
| An annulation reaction for the synthesis of morpholines, thiomorpholines, and piperazines from beta-heteroatom amino compounds and vinyl sulfonium salts. | 2008 |
|
| Isostructural materials achieved by using structurally equivalent donors and acceptors in halogen-bonded cocrystals. | 2008 |
|
| Morpholine-based immonium and halogenoamidinium salts as coupling reagents in Peptide synthesis1. | 2008 Apr 4 |
|
| Synthesis and in vitro anti-Helicobacter pylori activity of N-[5-(5-nitro-2-heteroaryl)-1,3,4-thiadiazol-2-yl]thiomorpholines and related compounds. | 2008 Aug |
|
| [Thiomorpholine transformation by the fungus Bjerkandera adusta]. | 2008 Sep-Oct |
|
| Synthesis and structure-activity relationship of dicationic diaryl ethers as novel potent anti-MRSA and anti-VRE agents. | 2009 Aug 15 |
|
| Manipulation of fluorescent and colorimetric changes of fluorescein derivatives and applications for sensing silver ions. | 2009 Mar 14 |
|
| Identification of advanced reaction products originating from the initial 4-oxo-2-nonenal-cysteine Michael adducts. | 2009 May |
|
| Synthetic studies of neoclerodane diterpenes from Salvia divinorum: role of the furan in affinity for opioid receptors. | 2009 Sep 21 |
|
| 2-(3-Oxo-3,4-dihydro-2H-1,4-benzo-thia-zin-4-yl)acetic acid monohydrate. | 2009 Sep 5 |
|
| N-heterocycle construction via cyclic sulfamidates. Applications in synthesis. | 2010 Apr 7 |
|
| One-pot multicomponent synthesis of two novel thiolactone scaffolds. | 2010 Aug |
|
| Artemisone effective against murine cerebral malaria. | 2010 Aug 9 |
|
| Syntheses and antibacterial activity studies of new oxazolidinones from nitroso Diels-Alder chemistry. | 2010 Feb 1 |
|
| Ethyl 4-hy-droxy-2,6-diphenyl-1-(2-thio-morpholino-acet-yl)-1,2,5,6-tetra-hydro-pyridine-3-carboxyl-ate. | 2010 Jul 10 |
|
| Phosphorescence imaging of homocysteine and cysteine in living cells based on a cationic iridium(III) complex. | 2010 Jul 19 |
|
| New benzofuran derivatives as an antioxidant agent. | 2010 Mar |
|
| Silica-supported fluoroboric acid (HBF(4)-SiO(2)) catalyzed highly productive synthesis of thiomorpholides as activators of l-asparaginase as well as the antioxidant agent. | 2010 May 15 |
|
| Turn-on luminescent probe for cysteine/homocysteine based on a ruthenium(II) complex. | 2010 Sep 6 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:42:59 GMT 2023
by
admin
on
Fri Dec 15 19:42:59 GMT 2023
|
| Record UNII |
3A8R61G6QV
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
67164
Created by
admin on Fri Dec 15 19:42:59 GMT 2023 , Edited by admin on Fri Dec 15 19:42:59 GMT 2023
|
PRIMARY | |||
|
m10722
Created by
admin on Fri Dec 15 19:42:59 GMT 2023 , Edited by admin on Fri Dec 15 19:42:59 GMT 2023
|
PRIMARY | Merck Index | ||
|
DTXSID80153826
Created by
admin on Fri Dec 15 19:42:59 GMT 2023 , Edited by admin on Fri Dec 15 19:42:59 GMT 2023
|
PRIMARY | |||
|
3A8R61G6QV
Created by
admin on Fri Dec 15 19:42:59 GMT 2023 , Edited by admin on Fri Dec 15 19:42:59 GMT 2023
|
PRIMARY | |||
|
C028971
Created by
admin on Fri Dec 15 19:42:59 GMT 2023 , Edited by admin on Fri Dec 15 19:42:59 GMT 2023
|
PRIMARY | |||
|
204-660-2
Created by
admin on Fri Dec 15 19:42:59 GMT 2023 , Edited by admin on Fri Dec 15 19:42:59 GMT 2023
|
PRIMARY | |||
|
THIOMORPHOLINE
Created by
admin on Fri Dec 15 19:42:59 GMT 2023 , Edited by admin on Fri Dec 15 19:42:59 GMT 2023
|
PRIMARY | |||
|
123-90-0
Created by
admin on Fri Dec 15 19:42:59 GMT 2023 , Edited by admin on Fri Dec 15 19:42:59 GMT 2023
|
PRIMARY | |||
|
36392
Created by
admin on Fri Dec 15 19:42:59 GMT 2023 , Edited by admin on Fri Dec 15 19:42:59 GMT 2023
|
PRIMARY |