Basic information Application Safety Supplier Related

6-Nitro-1,2-benzisothiazolin-3-one 1,1-dioxide

Basic information Application Safety Supplier Related

6-Nitro-1,2-benzisothiazolin-3-one 1,1-dioxide Basic information

Product Name:
6-Nitro-1,2-benzisothiazolin-3-one 1,1-dioxide
Synonyms:
  • 6-Nitro-1,1-dioxo-1,2-benzothiazol-3-one
  • 6-Nitro-1,2-benzisothiazol-3(2H)-one 1,1-dioxide
  • 6-Nitro-1,2-benzisothiazolin-3-one 1,1-dioxide
  • Nitrosaccharin
  • 6-nitro-2,3-dihydro-1$l^{6},2-benzothiazole-1,1,3-trione
  • 1,2-Benzisothiazol-3(2H)-One,6-Nitro,1,1-Dioxide
  • 6-Nitrobenzo[d]isothiazol-3(2H)-one 1,1-dioxide
  • 6-Nitrosaccharin
CAS:
22952-24-5
MF:
C7H4N2O5S
MW:
228.18
Mol File:
22952-24-5.mol
More
Less

6-Nitro-1,2-benzisothiazolin-3-one 1,1-dioxide Chemical Properties

Melting point:
205-207 °C
Density 
1.762±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
0?+-.0.30(Predicted)
color 
Off-white
CAS DataBase Reference
22952-24-5(CAS DataBase Reference)
More
Less

Safety Information

HS Code 
2934208090
More
Less

6-Nitro-1,2-benzisothiazolin-3-one 1,1-dioxide Usage And Synthesis

Application

6-Nitro-1,2-benzisothiazolin-3-one 1,1-dioxide is an organic intermediate that can be prepared from p-nitrotoluene in two steps. It has been reported in the literature as a potential candidate for synthesizing novel probes based on spatially induced electron transfer (SPET).

Synthesis

6269-91-6

22952-24-5

General procedure for the synthesis of 6-nitro-1,2-benzisothiazolin-3-one 1,1-dioxide from 2-methyl-5-nitrobenzenesulfonamide: A solution of chromium trioxide (20.4 g, 0.204 mol) in water (150 mL) was added drop-wise to concentrated sulfuric acid (190 mL) under ice-bath conditions. Subsequently, 2-methyl-5-nitrobenzenesulfonamide (10 g, 46.3 mmol) was added and the reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the mixture was filtered and the residue was washed with water and then dissolved in sodium bicarbonate solution and filtered again under vacuum. The filtrate was acidified with concentrated hydrochloric acid to precipitate. The precipitated product was collected by filtration and washed with plenty of cold water. Finally, the product was dried in a vacuum oven at 40°C to give a white powder in 72% yield. The melting point of the product was 205.6-205.8 °C (literature value: 205-207 °C); IR spectra showed characteristic absorption peaks located at 3103, 1720, 1608, 1541, 1354, 1340, 1184, 1128 cm-1 ; 1H NMR (DMSO-d6, 300 MHz) δ/ ppm: 8.02 (1H, d, J = 8.5 Hz), 8.56 (1H, d, J = 8.2 Hz), 8.71 (1H, s), 10.2 (1H, br, NH); 13C NMR (DMSO-d6, 75 MHz) δ/ ppm: 117.2, 126.4, 129.8, 135.2, 143.0, 151.7, 162.2.

References

[1] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 9, p. 2811 - 2821
[2] Asian Journal of Chemistry, 2017, vol. 29, # 7, p. 1622 - 1624
[3] Patent: WO2012/48222, 2012, A1. Location in patent: Page/Page column 98
[4] Tetrahedron, 2006, vol. 62, # 33, p. 7902 - 7910
[5] Bulletin of the Chemical Society of Japan, 1982, vol. 55, # 12, p. 3824 - 3827

6-Nitro-1,2-benzisothiazolin-3-one 1,1-dioxideSupplier

Beijing Ouhe Technology Co., Ltd
Tel
010-010-82967028 13522913783
Email
2355560935@qq.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Email
info@yuhaochemical.com
Shanghai Topbiochem Technology Co., Ltd
Tel
021-58170097
Email
info@topbiochem.com
9ding chemical ( Shanghai) Limited
Tel
4009209199
Email
sales@9dingchem.com