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7-Benzothiazolamine (9CI) is a benzothiazole derivative with the molecular formula C7H6N2S. It is a chemical compound that exhibits diverse biological activities and is used in the synthesis of organic compounds and pharmaceuticals. Its potential applications in medicine and agriculture are attributed to its antimicrobial, antifungal, and anti-inflammatory properties, making it a promising candidate for drug development. Additionally, 7-Benzothiazolamine (9CI) serves as a fluorescent dye in research and industrial applications due to its ability to emit bright fluorescence under ultraviolet light.

1123-55-3

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1123-55-3 Usage

Uses

Used in Pharmaceutical Industry:
7-Benzothiazolamine (9CI) is used as an active pharmaceutical ingredient for its antimicrobial, antifungal, and anti-inflammatory properties. It is employed in the development of drugs targeting various infections and inflammatory conditions.
Used in Agricultural Industry:
In agriculture, 7-Benzothiazolamine (9CI) is used as a bioactive compound for its potential applications in controlling plant pathogens and pests, thereby contributing to crop protection and yield enhancement.
Used in Research and Development:
7-Benzothiazolamine (9CI) is used as a fluorescent dye in research applications, where its bright fluorescence under ultraviolet light aids in the visualization and analysis of biological samples and materials.
Used in Industrial Applications:
In the industrial sector, 7-Benzothiazolamine (9CI) is utilized as a fluorescent marker in various processes, including quality control, product inspection, and safety testing, due to its distinctive fluorescent properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1123-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1123-55:
(6*1)+(5*1)+(4*2)+(3*3)+(2*5)+(1*5)=43
43 % 10 = 3
So 1123-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2S/c8-5-2-1-3-6-7(5)10-4-9-6/h1-4H,8H2

1123-55-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzo[d]thiazol-7-amine

1.2 Other means of identification

Product number -
Other names 1,3-benzothiazol-7-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1123-55-3 SDS

1123-55-3Relevant academic research and scientific papers

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

Rolli, Enrico,Incerti, Matteo,Brunoni, Federica,Vicini, Paola,Ricci, Ada

, p. 159 - 165 (2012/03/27)

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.

HETEROAROMATIC UREAS WHICH MODULATE THE FUNCTION OF THE VANILLOID-1 RECEPTOR (VR1)

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Page/Page column 41-42, (2010/02/11)

Compounds of formula (I): are useful as therapeutic compounds, particularly in the treatment of pain and other conditions ameliorated by the modulation of the function of the vanilloid-1 receptor (VR1).

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

Gallagher, Peter T.,Iddon, Brian,Suschitzky, Hans

, p. 2358 - 2361 (2007/10/02)

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.

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