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Key Documents

534242

Sigma-Aldrich

Thiazolo[2,3-b]benzimidazole-3(2H)-one

97%

Synonym(s):

Benzo[4,5]imidazo[2,1-b]thiazol-3-one

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About This Item

Empirical Formula (Hill Notation):
C9H6N2OS
CAS Number:
Molecular Weight:
190.22
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

97%

mp

180-184 °C (lit.)

SMILES string

O=C1CSc2nc3ccccc3n12

InChI

1S/C9H6N2OS/c12-8-5-13-9-10-6-3-1-2-4-7(6)11(8)9/h1-4H,5H2

InChI key

CFXICROPFOOZFI-UHFFFAOYSA-N

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - 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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D Galanakis et al.
Journal of medicinal chemistry, 38(4), 595-606 (1995-02-17)
Small conductance Ca(2+)-activated K+ (SKCa) channels occur in many cells but have been relatively little studied. Dequalinium, a bis-quinolinium compound, has recently been shown to be the most potent nonpeptidic blocker of this K+ channel subtype. This paper examines the
W A Bolhofer et al.
Journal of medicinal chemistry, 26(4), 538-544 (1983-04-01)
A series of aminoalkyl-substituted pyridylureas has been prepared and evaluated as inhibitors of gastric acid secretion. N,N-Dimethyl-N'-[2-(diisopropylamino)ethyl]-N'-(4,6-dimethyl-2-pyridyl)urea (8g) was the most potent example of the class. Comparison of this compound with cimetidine showed it to be equipotent in dogs stimulated
Celia Suárez-Pantaleón et al.
Organic & biomolecular chemistry, 9(13), 4863-4872 (2011-05-13)
To obtain highly-specific and selective forchlorfenuron binders, a collection of functionalized derivatives with different spacer arm locations and lengths was prepared. By immunization with target-mimicking haptens, a large battery of monoclonal and polyclonal antibodies against this synthetic cell regulator was

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