469114
6-硝基苯并噻唑
99%
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关于此项目
经验公式（希尔记法）:
C7H4N2O2S
化学文摘社编号:
分子量:
180.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-933-9
MDL number:
Assay:
99%
InChI key
QLUFBCVWKTWKBF-UHFFFAOYSA-N
InChI
1S/C7H4N2O2S/c10-9(11)5-1-2-6-7(3-5)12-4-8-6/h1-4H
SMILES string
[O-][N+](=O)c1ccc2ncsc2c1
assay
99%
mp
175-178 °C (lit.)
functional group
nitro
Quality Level
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Assignment of quaternary carbons in aromatic compounds by long-range heteronuclear shift correlated 2D-NMR spectroscopy and its application to acteoside.
Numata A, et al.
Agricultural and Biological Chemistry, 51(4), 1199-1201 (1987)
Heterocyclic Amplifiers of Phleomycin. IX. Some Derivatives of Fused and Unfused Mono-and Di-aza Heterocycles.
Barlin GB and Ireland SJ.
Australian Journal of Chemistry, 38(11), 1685-1691 (1985)
Livio Racané et al.
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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