CAS 136-95-8
:2-Aminobenzothiazole
Description:
2-Aminobenzothiazole is an organic compound characterized by its fused benzene and thiazole rings, featuring an amino group at the second position of the benzothiazole structure. It appears as a yellow to brown solid and is known for its heterocyclic nature, which contributes to its diverse chemical reactivity. This compound is soluble in polar solvents like water and alcohols, while being less soluble in non-polar solvents. 2-Aminobenzothiazole is primarily utilized in the synthesis of various dyes, pharmaceuticals, and agrochemicals, owing to its ability to participate in electrophilic substitution reactions. Additionally, it exhibits biological activity, including antimicrobial and antifungal properties, making it of interest in medicinal chemistry. Safety considerations are important, as it may pose health risks upon exposure, necessitating appropriate handling and storage measures. Overall, 2-Aminobenzothiazole is a valuable compound in both industrial and research applications due to its unique structural features and reactivity.
Formula:C7H6N2S
InChI:InChI=1/C7H6O3/c8-5-1-2-6-7(3-5)10-4-9-6/h1-3,8H,4H2
InChI key:InChIKey=UHGULLIUJBCTEF-UHFFFAOYSA-N
SMILES:NC1=NC=2C(S1)=CC=CC2
Synonyms:- 1,3-Benzodioxol-5-Ol
- 1,3-Benzothiazol-2-Amine
- 1,3-Benzothiazol-2-ylamine
- 2(3H)-Benzothiazolimine
- 2-Aminobenzo[d]thiazole
- 2-Aminobenzothiazol
- 2-Aminobenzthiazol
- 2-Benzothiazol amine
- 2-Benzothiazolamine
- 2-Benzothiazolylamine
- 2-Iminobenzothiazoline
- ABT
- Benzo[d]thiazol-2-amine
- Benzothiazol-2-Ylamine
- Benzothiazol-2-ylamin
- Benzothiazole, 1-amino-
- Benzothiazole, 2-amino-
- Benzothiazole-2-Ylamine
- Benzothiazoline, 2-imino-
- Benzotiazol-2-Ilamina
- Cerium ionophore I
- Nsc 4670
- Ska 1
- 2-Aminobenzothiazole
- 2-Aminobenzthiazole
- o-Aminobenzothiazole
- usafek-3941
- u-Aminoben-zothiazole
- CERIUM(III) IONOPHORE
- USAF EK-3941
- TIMTEC-BB SBB004071
- IFLAB-BB F1386-0409
- 2-amino-benzothiazol
- 3-AMINO BENZOTHIAZOLE
- USAF xr-27
- See more synonyms
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Found 14 products.
2-Aminobenzothiazole
CAS:Formula:C7H6N2SPurity:>97.0%(T)(HPLC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:150.202-Aminobenzothiazole, 98%
CAS:<p>2-Aminobenzothiazole was used in the synthesis of cobalt(II) picrate mixed-ligand complexes. It was used to study adsorption of biologically significant 2-aminobenzothiazole molecules on colloidal silver particles using surface-enhanced raman scattering spectroscopy This Thermo Scientific Chemicals </p>Formula:C7H6N2SPurity:98%Color and Shape:Powder, White to creamMolecular weight:150.202-Benzothiazolamine
CAS:<p>2-ABT: nitrogen-rich heterocycle used in drug synthesis, inhibits P450, with anti-inflammatory, anticonvulsant, anticancer properties.</p>Formula:C7H6N2SPurity:99.09% - 99.3%Color and Shape:Plates From Water Physical Description Odorless Gray To White Powder (Ntp 1992)Molecular weight:150.22-Aminobenzothiazole
CAS:Formula:C7H6N2SPurity:(HPLC) ≥ 98.0%Color and Shape:White to off-white or yellow powderMolecular weight:150.202-Amino-1,3-benzothiazole
CAS:<p>2-Amino-1,3-benzothiazole</p>Formula:C7H6N2SPurity:97%Color and Shape: faint beige solidMolecular weight:150.20g/mol2-Aminobenzothiazole
CAS:<p>Applications An impurity of pramipexole production<br>References Cressier, D., et al.: Bioorg. Med. Chem., 17, 5275 (2009), Suzuki, N., et al.: J. Med. Chem., 52, 2909 (2009), Xie, Y., et al.: Bioorg. Med. Chem. Lett., 19, 2354 (2009),<br></p>Formula:C7H6N2SColor and Shape:Off-WhiteMolecular weight:150.202-Aminobenzothiazole
CAS:Formula:C7H6N2SPurity:95%Color and Shape:Powder or Crystalline Powder or Solid or FlakesMolecular weight:150.22-Aminobenzothiazole
CAS:<p>2-Aminobenzothiazole is a nitrogen-containing organic compound that is used as an inhibitor in wastewater treatment. It has been shown to have antimicrobial properties in biological studies and is effective against gram-positive bacteria, including penicillin-resistant strains. The chemical structure of 2-aminobenzothiazole consists of a benzene ring with two amino groups attached to it. It has been shown that this compound binds to the enzyme ribonucleotide reductase and inhibits its activity, thereby preventing the production of RNA. The reaction mechanism for this inhibition is not yet known, although it may involve acid complex formation between 2-aminobenzothiazole and the enzyme.</p>Formula:C7H6N2SPurity:Min. 98.0 Area-%Color and Shape:PowderMolecular weight:150.2 g/mol












