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M6204

Sigma-Aldrich

2-Thiazoline-2-thiol

98%

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Synonym(s):
2-Mercapto-2-thiazoline
Empirical Formula (Hill Notation):
C3H5NS2
CAS Number:
Molecular Weight:
119.21
Beilstein:
106332
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

Signal Word

Danger

Hazard Statements

Precautionary Statements

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

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Chem. Abstr., 108, 37417r-37417r (1988)
Stud. Org. Chem., 28, 57-57 (1987)
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
Lei Tao et al.
Organic & biomolecular chemistry, 7(17), 3481-3485 (2009-08-14)
A novel thiazolidine-2-thione functionalized chain transfer agent (CTA) was synthesized and used as a reversible addition-fragmentation chain transfer (RAFT) polymerization agent to prepare well-defined poly-N-(2-hydroxypropyl) methacrylamide (PHPMA). The polymer chains had pre-designed molecular weights, narrow polydispersities and were chain-end functionalized.
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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