1123-55-3

Basic information

• Product Name: 7-Benzothiazolamine (9CI)
• Synonyms: 7-Benzothiazolamine (9CI);benzo[d]thiazol-7-amine;7-Benzothiazolamine;Benzothiazole-7-amine;7-Aminobenzothiazole;1,3-Benzothiazol-7-amine;7-Amino-1,3-benzothiazole
• CAS NO: 1123-55-3
• Molecular Formula: C₇H₆N₂S
• Molecular Weight: 150.20094
• Product Categories: BENZOTHIAZOLE
• Mol File: 1123-55-3.mol
• Article Data: 4

Chemical Properties

• Melting Point: 122-124℃
• Boiling Point: 323℃
• Flash Point: 149℃
• Appearance: Brown Solid
• Density: 1.383
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.763
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 4.44±0.30(Predicted)
• CAS DataBase Reference: 7-Benzothiazolamine (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Benzothiazolamine (9CI)(1123-55-3)
• EPA Substance Registry System: 7-Benzothiazolamine (9CI)(1123-55-3)

Safety Data

• Hazardous Substances Data: 1123-55-3(Hazardous Substances Data)

Usage

General Description

7-Benzothiazolamine (9CI) is a chemical compound with the molecular formula C7H6N2S. It is a benzothiazole derivative that is used in the synthesis of organic compounds and pharmaceuticals. This chemical has potential applications in the fields of medicine and agriculture due to its diverse biological activities. It has been studied for its antimicrobial, antifungal, and anti-inflammatory properties, making it a potential candidate for drug development. 7-Benzothiazolamine (9CI) is also used as a fluorescent dye in research and industrial applications, as it has the ability to emit bright fluorescence under ultraviolet light. Overall, this chemical compound has a variety of uses and potential benefits in different industries.

InChI:InChI=1/C7H6N2S/c8-5-2-1-3-6-7(5)10-4-9-6/h1-4H,8H2

Upstream product

• 2942-05-4 7-nitrobenzothiazole 
• 95-16-9 1,3-Benzothiazole 
• 149-30-4 2-Mercaptobenzothiazole 
• 3970-41-0 2-chloro-3-nitroaniline 

Downstream Products

• 848679-07-2 N-(1,3-benzothiazol-7-yl)-N'-[4-(trifluoromethyl)benzyl]urea 
• 1360448-91-4 1-(benzo[d]thiazol-7-yl)-3-phenylurea 
• 1298094-98-0 tetraphenyl (benzo[d]thiazol-7-ylamino)methylenediphosphonate 
• 700-48-1 4,6-Dibrombenzothiazol 
• 769-08-4 7-Amino-4-brombenzothiazol 
• 767-70-4 7-bromo-1,3-benzothiazole 
• 41228-99-3 2-benzothiazol-7-ylazo-4-methoxy-phenol 
• 41229-01-0 2-(benzothiazol-7-ylimino-methyl)-phenol 
• 99512-75-1 7-Acetamino-benzthiazol 

Relevant articles and documents

Structure-activity relationships of N-phenyl-N′-benzothiazol-6-ylurea synthetic derivatives: Cytokinin-like activity and adventitious rooting enhancement

Some years ago we demonstrated the cytokinin-like activity of the synthetic N-phenyl-N′-benzothiazol-6-ylurea (PBU) and a relevant adventitious rooting adjuvant activity of symmetric urea derivatives devoid of any cytokinin- or auxin-like activity per se. Here we report the synthesis and the biological activity evaluation of nine symmetric or asymmetric ureas/thioureas, structurally related to PBU. None of them show cytokinin-like activity, while we demonstrate for the first time that PBU interacts with Arabidopsis cytokinin receptor CRE1/AHK4 in a heterologous bioassay system. Among the PBU derivatives, all the symmetric ureas/thioureas show an adventitious rooting adjuvant activity in various bioassays, confirming that this activity is strictly dependent on their chemical structure.

Synthesis and Reactions of Azido-benzothiazoles and -benzothiophens; Novel Thiazolobenzoxazoles and Dihydrothienobenzoxazoles

6-Azidobenzothiazole and its 2-methyl and 2-methylthio-derivatives were prepared from the corresponding amine and gave the thiazolobenzoxazoles (8)-(10), on thermolysis in a polyphosphoric-acetic acid mixture. 6,7-Dihydro-2-methylthienobenzoxazole 8,8-dioxide (12) was prepared similarly.An improved method of synthesis of 2-fluoro-6-nitrobenzothiazole is reported.