Basic information Safety Supplier Related

5-Methyl-2-aminobenzothiazole

Basic information Safety Supplier Related

5-Methyl-2-aminobenzothiazole Basic information

Product Name:
5-Methyl-2-aminobenzothiazole
Synonyms:
  • 5-methyl-2-aminobenzothiazole
  • 2-AMINO-5-METHYLBENZOTHIAZOLE
  • 2-Benzothiazolamine,5-methyl-(9CI)
  • 5-Methyl-2-benzothiazolamine
  • 5-methylbenzo[d]thiazol-2-amine
  • 2-Benzothiazolamine,5-methyl-
  • 5-Methyl-2-benzo[d]thiazolamine
CAS:
14779-17-0
MF:
C8H8N2S
MW:
164.23
Product Categories:
  • BENZOTHIAZOLE
Mol File:
14779-17-0.mol
More
Less

5-Methyl-2-aminobenzothiazole Chemical Properties

Melting point:
182-184 °C(Solv: benzene (71-43-2))
Boiling point:
322.0±35.0 °C(Predicted)
Density 
1.315±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
4.31±0.10(Predicted)
Appearance
White to off-white Solid
CAS DataBase Reference
14779-17-0(CAS DataBase Reference)
More
Less

Safety Information

HS Code 
29342000
Toxicity
mouse,LD50,intravenous,74mg/kg (74mg/kg),Journal of Pharmacology and Experimental Therapeutics. Vol. 105, Pg. 486, 1952.
More
Less

5-Methyl-2-aminobenzothiazole Usage And Synthesis

Synthesis

333-20-0

108-44-1

14779-17-0

GENERAL METHOD: A solution of 3-methylaniline (2 mmol) in acetonitrile (15 ml) was added to a solution of potassium thiocyanate (8 mmol) in acetonitrile (15 ml). Subsequently, 0.06 g (30 mol% BF3) of BF3/SiO2 nanoparticles was added to the mixture and the mixture was placed in an ice salt bath and mechanically stirred for 30 min. Then, a solution of bromine (4 mmol, 0.2 ml) in acetonitrile (3 ml) was slowly added through a dropping funnel, controlling the rate of addition to ensure that the reaction temperature did not exceed 0 °C. After complete addition of bromine, the reaction mixture was 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 mixture was poured into water and heated to 70 °C on a steam bath followed by thermal filtration to remove the catalyst. The catalyst was washed with acetone and recycled for reuse. The filtrate was neutralized with 10% NaOH solution and the precipitate was collected, dried and recrystallized from ethanol (10 ml) to give 2-amino-5-methylbenzothiazole. The product was characterized by physical properties and spectral data (including melting point, FT-IR, 1H NMR and 13C NMR) and confirmed by comparison with known standards. Spectral data of the selected products: 6-bromo-1,3-benzothiazol-2-amine (2e) as a yellow solid; yield = 93%; melting point = 202-204 °C (literature value 203 °C); FT-IR (KBr) ν/cm-1: 3315, 3012, 2835, 1580, 1476, 1261, 920, 742, 512; 1H NMR ( 400MHz, CDCl3) δ ppm: 5.44 (s, 2H, NH2), 7.4-7.5 (d, 2H, Ar-H), 7.71 (s, 1H, Ar-H); 13C NMR (100MHz, DMSO-d6) δ ppm: 119, 120.9, 125.15, 126.07, 133.1, 152.15, 167.75. 152.15, 167.75.

References

[1] Research on Chemical Intermediates, 2016, vol. 42, # 12, p. 7855 - 7868
[2] Journal of Pharmaceutical Sciences, 1994, vol. 83, # 10, p. 1425 - 1432

5-Methyl-2-aminobenzothiazoleSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Email
info@chemlin.com.cn
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
China Langchem Inc.
Tel
0086-21-58956006