A80807
2-Amino-2-thiazoline
97%
Synonyme(s) :
2-Thiazolin-2-amine
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About This Item
Essai
97%
Pf
79-82 °C (lit.)
Chaîne SMILES
NC1=NCCS1
InChI
1S/C3H6N2S/c4-3-5-1-2-6-3/h1-2H2,(H2,4,5)
Clé InChI
REGFWZVTTFGQOJ-UHFFFAOYSA-N
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Code de la classe de stockage
13 - Non Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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Preliminary clinical results with norgamem (thioproline) and revercan (2-amino-2-thiazoline): the first inducers of reverse transformation.
Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer, 80, 346-350 (1982-01-01)
Nauchnye doklady vysshei shkoly. Biologicheskie nauki, (5)(5), 34-36 (1984-01-01)
The influence of 2-amino-2-thiazoline on the level of total sulphydryl groups in the haploid and diploid yeast cells Saccharomyces cerevisiae and Pichia guilliermondii has been studied. The increase of radioresistance of the yeast cells has been shown to be connected
Journal of inorganic biochemistry, 99(11), 2102-2109 (2005-09-08)
A new series of complexes of the type [Cu(dien)(2a-2tzn)Y(2)] and [Cu(dienXX)(2a-2tzn)Y(2)], where dien=diethylenetriamine and dienXX=Schiff dibase of diethylenetriamine formed with 2-furaldehyde (dienOO), 2-thiophenecarboxaldehyde (dienSS), or pyrrol-2-carboxaldehyde (dienNN); Y=Cl, Br or NO(3); and 2a-2tzn=2-amino-2-thiazoline, were synthesized and their structure established by
Arzneimittel-Forschung, 34(5), 599-603 (1984-01-01)
A series of derivatives of 4-arylthiazole acetic acid and 2-aminothiazole were studied with respect of their antiinflammatory effect in rat carrageenin edema. Some active compounds were found, which suppressed the paw edema formation strongly, and two compounds were selected, 4-(4-chlorophenyl)-2-phenylaminothiazole
Organic letters, 12(23), 5526-5529 (2010-11-03)
A series of 2-phenylaminothiazolines have been prepared from the corresponding N-(2-hydroxyethyl)-N'-phenylthioureas under mild reaction conditions using either thio-CDI (1,1'-thiocarbonyldiimidazole) or CDI (1,1'-carbonyldiimidazole) to promote the cyclization. This protocol provides the desired cyclization products in good yield with excellent selectivity. The
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