2-Amino-6-nitrobenzothiazole Chemical Properties

Melting point:

247-249 °C (lit.)

Boiling point:

411.7±37.0 °C(Predicted)

Density 

1.4666 (rough estimate)

refractive index 

1.6740 (estimate)

storage temp. 

2-8°C, protect from light

pka

1.76±0.10(Predicted)

Appearance

Light yellow to green yellow Solid

CAS DataBase Reference

6285-57-0(CAS DataBase Reference)

EPA Substance Registry System

2-Amino-6-nitrobenzothiazole (6285-57-0)

Safety Information

Hazard Codes 

Xn,Xi

Risk Statements 

20/21/22-36/37/38

Safety Statements 

26-36-36/37/39

RIDADR 

UN 2811 6.1/PG 3

WGK Germany 

2

RTECS 

DL0865000

TSCA 

Yes

HazardClass 

6.1

PackingGroup 

III

HS Code 

29342080

MSDS

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2-Amino-6-nitrobenzothiazole Usage And Synthesis

Chemical Properties

yellow crystalline powder

Uses

2-Amino-6-nitrobenzothiazole has been used:

• as model analyte for voltammetric determination of electrochemically reducible organic substances
• in the synthesis of 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid[2-(cyclohexanecarbonylamino)benzothiazol-6-yl]amide derivatives
• in the preparation of push-pull nonlinear optical chromophores containing thiazole and benzothiazole acceptors
• as a base in dye production by diazotation reaction

General Description

Orange crystals or yellow powder.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

2-Amino-6-nitrobenzothiazole is incompatible with strong oxidizing agents and strong acids.

Fire Hazard

Flash point data for 2-Amino-6-nitrobenzothiazole are not available; however, 2-Amino-6-nitrobenzothiazole is probably combustible.

Synthesis

GENERAL METHOD: A solution of 4-nitroaniline (2 mmol) in acetonitrile (15 ml) was slowly added to a solution of potassium thiocyanate (8 mmol) in acetonitrile (15 ml). Subsequently, 0.06 g (30 mol%) of BF3/SiO2 nanocatalyst was added to the reaction system and the mixture was placed in an ice salt bath and mechanically stirred for 30 min. A solution of bromine (4 mmol, 0.2 ml) in acetonitrile (3 ml) was slowly added through a dropping funnel, and the dropping rate was controlled to ensure that the reaction temperature did not exceed 0 °C. After the addition of the bromine solution, the reaction continued to be stirred at room temperature for 4 h, during which the progress of the reaction was monitored by TLC. Upon completion of the reaction, the reaction mixture was poured into water, heated in a 70 °C water bath and thermally filtered to remove the catalyst. The catalyst was washed with acetone and recycled for reuse. The filtrate was neutralized to neutrality with 10% NaOH solution and the precipitated solid was collected by filtration, dried and recrystallized with ethanol (10 ml) to give the target product 2-amino-6-nitrobenzothiazole. The structure of the product was confirmed by the following physical and spectral data and verified by comparison with standards. Spectral data of 2-amino-6-nitrobenzothiazole: yellow solid; yield = 93%; melting point = 202-204 °C (literature value 203 °C); FT-IR (KBr, cm^-1): 3315, 3012, 2835, 1580, 1476, 1261, 920, 742, 512; ^1H NMR (400 MHz, CDCl3 , δ ppm): 5.44 (s, 2H, NH2), 7.4-7.5 (d, 2H, Ar-H), 7.71 (s, 1H, Ar-H); ^13C NMR (100 MHz, DMSO-d6, δ ppm): 119, 120.9, 125.15, 126.07, 133.1, 152.15, 167.75.

References

[1] Synlett, 2012, vol. 23, # 15, p. 2219 - 2222
[2] Research on Chemical Intermediates, 2016, vol. 42, # 12, p. 7855 - 7868
[3] European Journal of Medicinal Chemistry, 2008, vol. 43, # 5, p. 1114 - 1122
[4] European Journal of Medicinal Chemistry, 2012, vol. 53, p. 41 - 51
[5] Russian Journal of Applied Chemistry, 2015, vol. 88, # 12, p. 2065 - 2073

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