Production Method 1

2516-37-2

945400-80-6

Reaction Conditions

1.1 Reagents: Iron Solvents: Acetic acid ;  16 h, rt

Reference

Preparation of hydrazone compound having (hetero)aryl group at terminal amine group for treating tau protein-associated disease

, Korea, , ,

Production Method 2

2516-37-2

945400-80-6

Reaction Conditions

1.1 Reagents: Iron Solvents: Acetic acid ;  24 h, rt

Reference

Preparation of imidazole derivatives as antiviral agents

, World Intellectual Property Organization, , ,

Production Method 3

2516-37-2

945400-80-6

Reaction Conditions

1.1 Reagents: Ferrous chloride ,  Sodium borohydride Solvents: Acetonitrile ;  14 h, 26 °C
1.2 Reagents: Water

Reference

Preparation of aryl amines via reduction of aromatic nitro compounds

, China, , ,

Production Method 4

2516-37-2

945400-80-6

Reaction Conditions

1.1 Reagents: Iron ,  Ammonium chloride Solvents: Ethanol ,  Water ;  2 - 3 h, 100 °C

Reference

Derivative with uracil-benzothiazole structures for treating hepatitis C

, China, , ,

Production Method 5

2516-37-2

945400-80-6

Reaction Conditions

1.1 Reagents: Iron Solvents: Acetic acid ;  6.5 h, rt

Reference

Preparation of heteroarylbenzothiazoles for imaging of amyloid deposits and treatment of Alzheimer's disease.

, World Intellectual Property Organization, , ,

Production Method 6

945400-80-6

Reaction Conditions

Reference

Novel heteroaryl substituted benzothiazoles

, United States, , ,

2-bromo-1,3-benzothiazol-6-amine Raw materials

• 2-bromo-6-nitro-1,3-benzothiazole

2-bromo-1,3-benzothiazol-6-amine Preparation Products

• 2-bromo-1,3-benzothiazol-6-amine (945400-80-6)

• 1. An Aptamer Bio-barCode (ABC) assay using SPR, RNase H, and probes with RNA and gold-nanorods for anti-cancer drug screening
  Chengbin Yang,Hing Lun Tsang,Pui Man Lau,Ken-Tye Yong,Ho Pui Ho,Siu Kai Kong Analyst, 2017,142, 3579-3587
• 2. An atomically efficient, highly stable and redox active Ce0.5Tb0.5Ox (3% mol.)/MgO catalyst for total oxidation of methane?
  Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
• 3. An assay for the enzyme N-acetyl-β-d-glucosaminidase (NAGase) based on electrochemical detection using screen-printed carbon electrodes (SPCEs)
  R. M. Pemberton,J. P. Hart,T. T. Mottram Analyst, 2001,126, 1866-1871
• 4. An amorphous carbon nitride/NiO/CoN-based composite: a highly efficient nonprecious electrode for supercapacitors and the oxygen evolution reaction?
  Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
• 5. An insight into the origin of room-temperature ferromagnetism in SnO2 and Mn-doped SnO2 quantum dots: an experimental and DFT approach?
  Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Benzothiazoles Benzothiazoles
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Benzothiazoles

• 408328-13-2(2,6-Dibromobenzothiazole)
• 533-30-2(1,3-Benzothiazol-6-amine)
• 2516-40-7(2-Bromo-1,3-benzothiazole)
• 3507-44-6(2-Bromo-5-NitrobenzoDThiazole)
• 1019111-64-8(2,5-Dibromo-benzothiazole)
• 412923-50-3(2-Bromo-6-ethylbenzothiazole)
• 1093107-11-9(2-bromo-5-methyl-1,3-benzothiazole)
• 3622-19-3(2-Bromo-6-methylbenzodthiazole)
• 2516-37-2(2-bromo-6-nitro-1,3-benzothiazole)
• 1206250-69-2(2-Bromothiazolo[5,4-c]pyridine)