5-NITROBENZOTHIAZOLE
- Product Name
- 5-NITROBENZOTHIAZOLE
- CAS No.
- 2942-07-6
- Chemical Name
- 5-NITROBENZOTHIAZOLE
- Synonyms
- 5-NITROBENZOTHIAZOLE;Benzothiazole,5-nitro-;5-Nitrobenzothiazole,96%;5-nitro-1,3-benzothiazole;Benzothiazole, 5-nitro- (6CI,7CI,8CI,9CI)
- CBNumber
- CB0195324
- Molecular Formula
- C7H4N2O2S
- Formula Weight
- 180.18
- MOL File
- 2942-07-6.mol
5-NITROBENZOTHIAZOLE Property
- Melting point:
- 163-164℃
- Boiling point:
- 333.7±15.0 °C(Predicted)
- Density
- 1.525±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- -0.87±0.10(Predicted)
- Appearance
- White to yellow Solid
- CAS DataBase Reference
- 2942-07-6
Safety
- HazardClass
- IRRITANT
- HS Code
- 2934999090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405Store locked up.
N-Bromosuccinimide Price
- Product number
- W5193
- Product name
- 5-Nitrobenzothiazole
- Packaging
- 1g
- Price
- $108
- Updated
- 2021/12/16
- Product number
- 8H70-1-96
- Product name
- 5-Nitrobenzothiazole
- Packaging
- 1g
- Price
- $221
- Updated
- 2021/12/16
- Product number
- 059193
- Product name
- 5-Nitro-benzothiazole
- Purity
- 95+%
- Packaging
- 1g
- Price
- $360
- Updated
- 2021/12/16
- Product number
- 8H70-1-96
- Product name
- 5-Nitrobenzothiazole
- Packaging
- 5G
- Price
- $871
- Updated
- 2021/12/16
- Product number
- CHM0077123
- Product name
- 5-NITROBENZOTHIAZOLE
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $972.51
- Updated
- 2021/12/16
5-NITROBENZOTHIAZOLE Chemical Properties,Usage,Production
Chemical Properties
Yellow solid
Synthesis
758-16-7
97-00-7
2942-07-6
General procedure for the synthesis of 5-nitrobenzothiazole from dimethylthiocarbamide and 2,4-dinitrochlorobenzene: 1-chloro-2,4-dinitrobenzene (8 g, 39 mmol) was mixed with N,N-dimethylthiocarbamide (14.5 ml, 178 mmol) and heated to react for 3 hr at 60 °C, during which a yellow precipitate was produced. Subsequently, xylene (20 ml) was added to the reaction mixture and the mixture was heated to reflux for 4 hours, after which stirring was continued for 18 hours at room temperature. After completion of the reaction, the mixture was diluted with ethanol (12 ml), filtered and the solid was washed with minimum amount of ethanol. The brown solid obtained was dissolved in ethanol (100 ml), heated to boiling and thermally filtered. The filtrate was concentrated to about 80 ml and left at room temperature overnight. Finally, the precipitated solid was collected by filtration and washed with ethanol to give 1.9 g (32% yield) of 5-nitro-1,3-benzothiazole. The structure of the product was confirmed by 1H NMR (CDCl3): δ 8.11 (1H, d, J=8.6 Hz), 8.36 (1H, dd, J=2.2, 8.8 Hz), 9.01 (1H, d, J=2.0 Hz), 9.20 (1H, s).
References
[1] Patent: WO2005/28445, 2005, A2. Location in patent: Page/Page column 27-28
[2] Patent: US2001/345, 2001, A1
5-NITROBENZOTHIAZOLE Preparation Products And Raw materials
Raw materials
Preparation Products
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