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Quality Level
Assay
99%
mp
175-178 °C (lit.)
SMILES string
[O-][N+](=O)c1ccc2ncsc2c1
InChI
1S/C7H4N2O2S/c10-9(11)5-1-2-6-7(3-5)12-4-8-6/h1-4H
InChI key
QLUFBCVWKTWKBF-UHFFFAOYSA-N
General description
The XCORFE (Xnucleus-proton correlation with fixed evolution time) pulse sequence of 6-nitrobenzothiazole has been tested.
Application
6-Nitrobenzothiazole may be used in the preparation of 4-amino-3-sulfanylbenzonitrile and 2-amino-5-nitrobenzothiole, via alkaline hydrolysis.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
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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Heterocyclic Amplifiers of Phleomycin. IX. Some Derivatives of Fused and Unfused Mono-and Di-aza Heterocycles.
Australian Journal of Chemistry, 38(11), 1685-1691 (1985)
Assignment of quaternary carbons in aromatic compounds by long-range heteronuclear shift correlated 2D-NMR spectroscopy and its application to acteoside.
Agricultural and Biological Chemistry, 51(4), 1199-1201 (1987)
Bioorganic & medicinal chemistry, 18(3), 1038-1044 (2010-01-12)
The efficient synthesis of new bis-substituted nitro-amidino, amino-amidino (10a, 10b-13a, 13b) and previously prepared diamidino 2-phenyl-benzothiazoles (9a, 9b) is described. The compounds 11a and 11b were prepared by recently developed methodology of the key precursors in zwitterionic form 8a and
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