2-Amino-6-methoxybenzothiazoleCAS# 1747-60-0 |
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| Cas No. | 1747-60-0 | SDF | Download SDF |
| PubChem ID | 15630 | Appearance | Powder |
| Formula | C8H8N2OS | M.Wt | 180 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 6-methoxy-1,3-benzothiazol-2-amine | ||
| SMILES | COC1=CC2=C(C=C1)N=C(S2)N | ||
| Standard InChIKey | KZHGPDSVHSDCMX-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C8H8N2OS/c1-11-5-2-3-6-7(4-5)12-8(9)10-6/h2-4H,1H3,(H2,9,10) | ||
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
||
| About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
||
| Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. | ||
2-Amino-6-methoxybenzothiazole Dilution Calculator
2-Amino-6-methoxybenzothiazole Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 5.5556 mL | 27.7778 mL | 55.5556 mL | 111.1111 mL | 138.8889 mL |
| 5 mM | 1.1111 mL | 5.5556 mL | 11.1111 mL | 22.2222 mL | 27.7778 mL |
| 10 mM | 0.5556 mL | 2.7778 mL | 5.5556 mL | 11.1111 mL | 13.8889 mL |
| 50 mM | 0.1111 mL | 0.5556 mL | 1.1111 mL | 2.2222 mL | 2.7778 mL |
| 100 mM | 0.0556 mL | 0.2778 mL | 0.5556 mL | 1.1111 mL | 1.3889 mL |
| * Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. | |||||
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- CH 275
Catalog No.:BCC5913
CAS No.:174688-78-9
- AN-2690
Catalog No.:BCC1360
CAS No.:174671-46-6
- Phalloidin
Catalog No.:BCC7945
CAS No.:17466-45-4
- Talnetant
Catalog No.:BCC1981
CAS No.:174636-32-9
- SB-222200
Catalog No.:BCC1926
CAS No.:174635-69-9
- SB 218795
Catalog No.:BCC7037
CAS No.:174635-53-1
- SDZ 220-040
Catalog No.:BCC6992
CAS No.:174575-40-7
- SDZ 220-581
Catalog No.:BCC1939
CAS No.:174575-17-8
- 2-Allylphenol
Catalog No.:BCC8518
CAS No.:1745-81-9
- alpha-Spinasterol glucoside
Catalog No.:BCN1120
CAS No.:1745-36-4
- Tipranavir
Catalog No.:BCC2002
CAS No.:174484-41-4
- Sanggenol A
Catalog No.:BCN3602
CAS No.:174423-30-4
- Ginsenoside Rh4
Catalog No.:BCN3503
CAS No.:174721-08-5
- Carabrone
Catalog No.:BCN1121
CAS No.:1748-81-8
- Fmoc-Hyp(Bzl)-OH
Catalog No.:BCC3255
CAS No.:174800-02-3
- 3-Amino-4-methoxybenzamide
Catalog No.:BCC8612
CAS No.:17481-27-5
- Rabdoketone B
Catalog No.:BCN6598
CAS No.:174819-51-3
- Parishin B
Catalog No.:BCN3812
CAS No.:174972-79-3
- Parishin C
Catalog No.:BCN3813
CAS No.:174972-80-6
- Tonabersat
Catalog No.:BCC2009
CAS No.:175013-84-0
- NQDI 1
Catalog No.:BCC2404
CAS No.:175026-96-7
- O4I1
Catalog No.:BCC6542
CAS No.:175135-47-4
- Xanthorin
Catalog No.:BCN1122
CAS No.:17526-15-7
- Fmoc-Thr(HPO3Bzl)-OH
Catalog No.:BCC3551
CAS No.:175291-56-2
Mixed ligand Cu(II)N2O2 complexes: biomimetic synthesis, activities in vitro and biological models, theoretical calculations.[Pubmed:25470554]
Inorg Chem. 2014 Dec 15;53(24):13019-30.
Three new mixed ligand Cu(II)N2O2 complexes, namely, [Cu(II)(2-A-6-MBT)2(m-NB)2] (1), [Cu(II)(2-ABT)2(m-NB)2] (2), and [Cu(II)(2-ABT)2(o-NB)2] (3), (2-A-6-MBT = 2-Amino-6-methoxybenzothiazole, m-NB = m-nitrobenzoate, 2-ABT = 2-aminobenzothiazole, and o-NB = o-nitrobenzoate), have been prepared by the biomimetic synthesis strategy, and their structures were determined by X-ray crystallography studies and spectral methods. These complexes exhibited the effective superoxide dismutase (SOD) activity and catecholase activity. On the basis of the experimental data and computational studies, the structure-activity relationship for these complexes was investigated. The results reveal that electron-accepting abilities of these complexes and coordination geometries have significant effects on the SOD activity and catecholase activity. Then, we found that 1 and 2 exerted potent intracellular antioxidant capacity in the model of H2O2-induced oxidative stress based on HeLa cervical cancer cells, which were screened out by the cytotoxicity assays of different kinds of cells. Furthermore, 1-3 showed the favorable biocompatibility in two different biological models: Saccharomyces cerevisiae and human vascular endothelial cells. These biological experimental data are indicative of the promising application potential of these complexes in biology and pharmacology.
Synthesis and antimicrobial activity of new 4-thiazolidinone derivatives containing 2-amino-6-methoxybenzothiazole.[Pubmed:23964172]
Saudi Pharm J. 2010 Jul;18(3):129-36.
A novel series of Schiff bases 5a-j and 4-thiazolidinones 6a-j have been prepared from the building blocks 2-chloro pyridine-3-carboxylic acid [1] and 2-amino-6-methoxy-benzothiazole [2]. All of the synthesized compounds have been confirmed by elemental analyses, IR, (1)H NMR and (13)C NMR spectral data. These newly synthesized compounds were screened for their antimicrobial activity. Variable and modest activity was observed against the investigated strains of bacteria and fungi, however, compound 6h revealed significant antibacterial activity against Escherichia coli. Compounds 1, 2, 3, 5c, 5g and 5h, on the other hand, revealed potent antifungal activity against Candida albicans compared to the reference drug greseofulvin.
