M6204
2-Thiazoline-2-thiol
98%
Synonym(s):
2-Mercapto-2-thiazoline
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About This Item
Empirical Formula (Hill Notation):
C3H5NS2
CAS Number:
Molecular Weight:
119.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-512-1
Beilstein/REAXYS Number:
106332
MDL number:
Assay:
98%
InChI
1S/C3H5NS2/c5-3-4-1-2-6-3/h1-2H2,(H,4,5)
InChI key
WGJCBBASTRWVJL-UHFFFAOYSA-N
SMILES string
S=C1NCCS1
assay
98%
Quality Level
mp
100-105 °C (lit.)
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Related Categories
Application
Tool for highly selective chiral syntheses of penam- and carbapenam-type β-lactam antibiotics.
signalword
Danger
hcodes
pcodes
Hazard Classifications
Acute Tox. 3 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Stud. Org. Chem., 28, 57-57 (1987)
R van Doorn et al.
Archives of toxicology, 47(1), 51-58 (1981-03-01)
A compound was isolated from the urine of workers exposed to carbon disulfide during the production of rayon. The compound was identified as 2-thiothiazolidine-4-carboxylic acid (TTCA) by GC/MS and NMR. A HPLC method for the quantitative determination of TTCA was
Y H Chen et al.
Chemosphere, 56(2), 133-140 (2004-05-04)
This study investigates the ozonation of 2-mercaptothiazoline (2-MT). The 2-MT is one of the important organic additives for the electroplating solution of the printed wiring board industry and has been widely used as a corrosion inhibitor in many industrial processes.
Yahia N Mabkhot et al.
Molecules (Basel, Switzerland), 24(9) (2019-05-01)
A series of new thiazoline derivatives were synthesized. Structure analyses were accomplished employing 1H-NMR, 13C-NMR, X-ray and MS techniques. The in vitro antitumor activities were assessed against human hepatocellular carcinoma (HepG-2) and colorectal carcinoma (HCT-116) cell lines. The results revealed
Damián Pérez-Quintanilla et al.
Journal of hazardous materials, 134(1-3), 245-256 (2005-12-06)
Mesoporous silicas (SBA-15 and MCM-41) have been functionalized by two different methods. Using the heterogeneous route the silylating agent, 3-chloropropyltriethoxysilane, was initially immobilized onto the mesoporous silica surface to give the chlorinated mesoporous silica Cl-SBA-15 or Cl-MCM-41. In a second
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