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2-(3,5-Dichloro-phenyl)-benzothiazole, commonly known as DCPTB, is a chemical compound with a molecular formula C13H7Cl2NS. It is a versatile compound known for its strong fluorescence, high thermal stability, and electron transport properties.

391219-75-3

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391219-75-3 Usage

Uses

Used in Analytical Chemistry:
2-(3,5-Dichloro-phenyl)-benzothiazole is used as a fluorescent probe for the detection of Hg(II) ions in aqueous media. Its strong fluorescence allows for sensitive and selective detection of mercury ions, making it a valuable tool in environmental and biological analysis.
Used in Material Science:
2-(3,5-Dichloro-phenyl)-benzothiazole is used as a potential OLED (Organic Light Emitting Diode) material due to its high thermal stability and electron transport properties. These characteristics make it a promising candidate for the development of advanced display technologies and lighting systems.
Used in Environmental Monitoring:
2-(3,5-Dichloro-phenyl)-benzothiazole is used as a sensor for detecting heavy metal ions in environmental and biological samples. Its ability to interact with and respond to the presence of these ions makes it a valuable tool for monitoring pollution and ensuring environmental safety.
Used in Pharmaceutical Development:
2-(3,5-Dichloro-phenyl)-benzothiazole is used as a potential candidate for the development of new pharmaceutical drugs due to its antimicrobial and antifungal properties. Its activity against various pathogens suggests that it could be a useful component in the fight against infectious diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 391219-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,1,2,1 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 391219-75:
(8*3)+(7*9)+(6*1)+(5*2)+(4*1)+(3*9)+(2*7)+(1*5)=153
153 % 10 = 3
So 391219-75-3 is a valid CAS Registry Number.

391219-75-3SDS

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 2-(3,5-dichlorophenyl)-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-(2,2-DIMETHYL-4-PHENYLTETRAHYDRO-2H-PYRAN-4-YL)ETHANAMINE

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:391219-75-3 SDS

391219-75-3Downstream Products

391219-75-3Relevant academic research and scientific papers

Copper-catalyzed double c-s bonds formation via different paths: Synthesis of benzothiazoles from n -benzyl-2-iodoaniline and potassium sulfide

Zhang, Xiaoyun,Zeng, Weilan,Yang, Yuan,Huang, Hui,Liang, Yun

supporting information, p. 876 - 879 (2014/03/21)

A new, highly efficient procedure for the synthesis of benzothiazoles from easily available N-benzyl-2-iodoaniline and potassium sulfide has been developed. The results show copper-catalyzed double C-S bond formation via a traditional cross-coupling reaction and an oxidative cross-coupling reaction.

Solid phase combinatorial synthesis of benzothiazoles and evaluation of topoisomerase II inhibitory activity

Choi, Suk-June,Park, Hyen Joo,Lee, Sang Kook,Kim, Sang Woong,Han, Gyoonhee,Choo, Hea-Young Park

, p. 1229 - 1235 (2007/10/03)

To investigate one possible mechanism of action of the cytotoxic activity of benzothiazoles, we synthesized 2-(substituted-phenyl)benzothiazoles and evaluated their ability to inhibit topoisomerase II activities. Solid phase combinatorial method using tri

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