Basic information Safety Supplier Related

6-Nitro-2-benzothiazolinone

Basic information Safety Supplier Related

6-Nitro-2-benzothiazolinone Basic information

Product Name:
6-Nitro-2-benzothiazolinone
Synonyms:
  • 6-NITRO-2-BENZOTHIAZOLINONE
  • 6-NITRO-BENZOTHIAZOL-2-ONE
  • 6-nitro-3H-1,3-benzothiazol-2-one
  • 6-nitro-2(3H)-benzothiazolone
  • 2(3H)-Benzothiazolone,6-nitro-(9CI)
  • 6-Nitro-2,3-dihydro-1,3-benzothiazol-2-one
  • 6-nitro-2H-benzothiazolinone
  • 6-Nitrobenzo[d]thiazol-2(3H)-one
CAS:
28620-12-4
MF:
C7H4N2O3S
MW:
196.18
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Building Blocks
  • Heterocyclic Building Blocks
  • Thiazolines/Thiazolidines
  • BENZOTHIAZOLE
Mol File:
28620-12-4.mol
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6-Nitro-2-benzothiazolinone Chemical Properties

Melting point:
246 °C (dec.) (lit.)
Density 
1.603±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
viscous liquid
pka
8.78±0.20(Predicted)
Appearance
Light yellow to yellow Solid
CAS DataBase Reference
28620-12-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
HS Code 
29342000

MSDS

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6-Nitro-2-benzothiazolinone Usage And Synthesis

Chemical Properties

White solid

Uses

6-Nitro-2-benzothiazolinone may be used as a starting reagent for the synthesis of 3-alkyl-6-nitro-2-benzothiazolinones.

General Description

6-Nitro-2-benzothiazolinone is a 6-substituted 2-benzothiazolinone.

Synthesis

934-34-9

28620-12-4

General procedure for the synthesis of 6-nitro-2-(3H)-benzothiazolone from 2-hydroxybenzothiazole: 3H-benzothiazol-2-one (10 g, 66 mmol) was added to 70% nitric acid (20 mL), and the reaction was stirred for 3 h at 20 °C. After completion of the reaction, the precipitate was collected by filtration and washed with deionized water. The crude product was purified by recrystallization from anhydrous ethanol. The yield of this synthesis step was 90% and the melting point of the product was 228-229 °C. It was characterized by 1H NMR (300 MHz, DMSO-d6): δ 7.28 (d, J = 8.9 Hz, 1H, H4), 8.18 (dd, J = 8.9 Hz, J = 2.4 Hz, 1H, H5), 8.65 (d, J = 2.5 Hz, 1H, H7), and 12.54 (br s, 1H, NH).13C NMR ( 75 MHz, DMSO-d6) characterization: δ 111.9 (CH), 119.6 (CH), 123.2 (CH), 125.0 (Caro), 142.5 (Caro), 142.9 (Caro), 171.0 (CO).LCMS (ESI-) analysis: calculated value of [M-H+] is 195.0; measured value is 195.0.

References

[1] European Journal of Medicinal Chemistry, 2015, vol. 92, p. 807 - 817
[2] Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1503 - 1509
[3] Monatshefte fur Chemie, 2011, vol. 142, # 1, p. 67 - 80
[4] Chemistry of Heterocyclic Compounds, 1990, vol. 25, # 11, p. 1294 - 1296
[5] Patent: US2003/40533, 2003, A1

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