A80807
2-Amino-2-thiazoline
97%
Synonym(s):
2-Thiazolin-2-amine
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About This Item
Empirical Formula (Hill Notation):
C3H6N2S
CAS Number:
Molecular Weight:
102.16
Beilstein/REAXYS Number:
105367
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
assay
97%
mp
79-82 °C (lit.)
SMILES string
NC1=NCCS1
InChI
1S/C3H6N2S/c4-3-5-1-2-6-3/h1-2H2,(H2,4,5)
InChI key
REGFWZVTTFGQOJ-UHFFFAOYSA-N
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Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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L T Zolotareva et al.
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
A Th Chaviara et al.
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
Preliminary clinical results with norgamem (thioproline) and revercan (2-amino-2-thiazoline): the first inducers of reverse transformation.
A Brugarolas et al.
Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer, 80, 346-350 (1982-01-01)
H Nagatomi et al.
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
April L Bernacki et al.
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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