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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
Structure of THIOMORPHOLINE

SMILES

C1CSCCN1

InChI

InChIKey=BRNULMACUQOKMR-UHFFFAOYSA-N
InChI=1S/C4H9NS/c1-3-6-4-2-5-1/h5H,1-4H2

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
New antibacterial tetrahydro-4(2H)-thiopyran and thiomorpholine S-oxide and S,S-dioxide phenyloxazolidinones.
2003 Dec 1
Importance of the thiomorpholine introduction in new pyrrole derivatives as antimycobacterial agents analogues of BM 212.
2003 Feb 20
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
Kinetics of degradation of sulphur mustard on impregnated carbons.
2005 May 20
Acetylenic TACE inhibitors. Part 3: Thiomorpholine sulfonamide hydroxamates.
2006 Mar 15
Selective phosphorescence chemosensor for homocysteine based on an iridium(III) complex.
2007 Dec 24
Ethyl 4-hydr-oxy-2,6-diphenyl-1-(2-thio-morpholinopropano-yl)-1,2,5,6-tetra-hydro-pyridine-3-carboxyl-ate.
2009 Nov 21
(R)-1-[(S)-(3-Cyano-thio-morpholino)carbon-yl]-2-methyl-propyl-aminium chloride dihydrate.
2009 Nov 28
N-heterocycle construction via cyclic sulfamidates. Applications in synthesis.
2010 Apr 7
One-pot multicomponent synthesis of two novel thiolactone scaffolds.
2010 Aug
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
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
4-(1H-Benzimidazol-2-ylmeth-yl)-2H-1,4-benzothia-zin-3(4H)-one.
2010 May 29
Turn-on luminescent probe for cysteine/homocysteine based on a ruthenium(II) complex.
2010 Sep 6
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:42:59 GMT 2023
Edited
by admin
on Fri Dec 15 19:42:59 GMT 2023
Record UNII
3A8R61G6QV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THIOMORPHOLINE
Systematic Name English
THIAMORPHOLINE [MI]
Common Name English
Code System Code Type Description
PUBCHEM
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
MERCK INDEX
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
EPA CompTox
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
FDA UNII
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
MESH
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
ECHA (EC/EINECS)
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
WIKIPEDIA
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
CAS
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
CHEBI
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