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M6204

Sigma-Aldrich

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:
96-53-7
Molecular Weight:
119.21
Beilstein:
106332
EC Number:
202-512-1
MDL number:
MFCD00126013
UNSPSC Code:
12352100
PubChem Substance ID:
24897083
NACRES:
NA.22

Quality Level

200

Assay

98%

mp

100-105 °C (lit.)

SMILES string

S=C1NCCS1

InChI

1S/C3H5NS2/c5-3-4-1-2-6-3/h1-2H2,(H,4,5)

InChI key

WGJCBBASTRWVJL-UHFFFAOYSA-N

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Application

Tool for highly selective chiral syntheses of penam- and carbapenam-type β-lactam antibiotics.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301

Precautionary Statements

P301 + P310

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Stud. Org. Chem., 28, 57-57 (1987)
J C Thomes et al.
Japanese journal of pharmacology, 58(3), 201-207 (1992-03-01)
2-Thiazoline-2-thiol is an antithyroid agent that strongly reduces thyroid hormone levels. Synthesis of these hormones is catalyzed in vivo by thyroid peroxidase. The interaction of this drug with molecular iodine and its effect on peroxidase activity were investigated. Iodine and
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