CAS 1747-60-0
:2-Amino-6-metossibenzotiazolo
- (6-Methoxybenzothiazol-2-yl)amine
- 2-Amino-4,5,6,7-Tetrahydro-1-Benzothiophene-3-Carbonitrile
- 2-Amino-6-methoxy benzothiazole
- 2-Benzothiazolamine, 6-methoxy-
- 3'-Chlorobiphenyl-4-Carbaldehyde
- 3'-Methoxybiphenyl-4-Carbaldehyde
- 3'-Methylbiphenyl-4-Carbaldehyde
- 3-chloro-N-(3-cyano-4,5,6,7-tetrahydro-1-benzothiophen-2-yl)propanamide
- 6-(Methyloxy)-1,3-benzothiazol-2-amine
- 6-Methoxy-1,3-Benzothiazol-2-Amine
- 6-Methoxy-1,3-Benzothiazol-2-Amine Sulfate (1:1)
- 6-Methoxy-1,3-benzothiazol-2-ylamine
- 6-Methoxy-2-aminobenzothiazole
- 6-Methoxy-2-benzothiazolamine
- 6-Methoxybenzo[D]Thiazol-2-Amine
- 6-Methoxybenzothiazol-2-Ylamine
- Benzothiazole, 2-amino-6-methoxy-
- NSC 27516
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2-Amino-6-methoxybenzothiazole
CAS:Formula:C8H8N2OSPurezza:>98.0%(T)Colore e forma:White to Gray to Brown powder to lumpPeso molecolare:180.232-Amino-6-methoxybenzothiazole, 98%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo SciFormula:C8H8N2OSPurezza:98%Colore e forma:Cream to pale brown, PowderPeso molecolare:180.236-methoxybenzo[d]thiazol-2-amine
CAS:Formula:C8H8N2OSPurezza:96%Colore e forma:SolidPeso molecolare:180.22692-Amino-6-methoxy-1,3-benzothiazole
CAS:2-Amino-6-methoxy-1,3-benzothiazoleFormula:C8H8N2OSPurezza:techColore e forma:SolidPeso molecolare:180.226922-Amino-6-methoxybenzothiazole
CAS:2-Amino-6-methoxybenzothiazoleFormula:C8H8N2OSPurezza:97%Peso molecolare:180.232-Amino-6-methoxybenzothiazole
CAS:2-Amino-6-methoxybenzothiazole is a drug that is used to treat cervical cancer. It has inhibitory properties against the growth of human tumor cells in vitro. The inhibition of cell proliferation was shown to be mediated by the hydroxyl group, which interacts with the methyl ketones, leading to a decrease in the Langmuir adsorption isotherm. 2-Amino-6-methoxybenzothiazole also inhibits sodium carbonate and hydrochloric acid, which are important for transcription and translation of DNA. This drug has been shown to have no effect on proton NMR spectra or amines, but does react with coumarin derivatives. The reaction mechanism may involve an inorganic acid such as nitric acid or phosphoric acid.
Formula:C8H8N2OSPurezza:Min. 95%Peso molecolare:180.23 g/mol2-Amino-6-methoxybenzothiazole
CAS:Formula:C8H8N2OSPurezza:96%Colore e forma:SolidPeso molecolare:180.232-Amino-6-methoxybenzothiazole
CAS:Prodotto controllatoApplications 2-Amino-6-methoxybenzothiazole is an intermediate used to prepare novel series of Schiff bases and 4-thiazolidinones. It is also used in the synthesis of 2-cyano-6-methoxybenzothiazole.
References Patel, N., et al.: Saudi Pharma. J., 18, 129 (2010); Toya, Y., et al.: Bull. Chem. Soc. Jpn., 65, 392 (1992)Formula:C8H8N2OSColore e forma:NeatPeso molecolare:180.23








