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2-(2,6-dichlorophenyl)-1,3-benzothiazole is a chemical compound with the molecular formula C13H6Cl2NS. It is a derivative of benzothiazole, which is a heterocyclic compound consisting of a benzene ring fused to a thiazole ring. The compound is characterized by the presence of two chlorine atoms attached to the 2 and 6 positions of the phenyl group, which is connected to the benzothiazole core. This specific chemical structure endows it with unique properties, making it useful in various applications such as in the synthesis of pharmaceuticals, agrochemicals, and as a building block in the development of new materials. Its chemical reactivity and stability are influenced by the electron-withdrawing nature of the chlorine atoms and the aromaticity of the benzene and thiazole rings.

15952-10-0

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15952-10-0 Usage

Usage

DBx is used as a fluorescent brightener, commonly added to plastics, fibers, and coatings to enhance their whiteness and brightness.

Additional Benefits

DBx is also used in the manufacturing of polymers and rubber products to provide UV protection and to inhibit yellowing.

Safety Measures

Proper safety measures should be taken when handling and using DBx in industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 15952-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,5 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15952-10:
(7*1)+(6*5)+(5*9)+(4*5)+(3*2)+(2*1)+(1*0)=110
110 % 10 = 0
So 15952-10-0 is a valid CAS Registry Number.

15952-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6-Dichlorophenyl)-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names Benzothiazole,2-(2,6-dichlorophenyl)

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:15952-10-0 SDS

15952-10-0Downstream Products

15952-10-0Relevant academic research and scientific papers

Fe3O4@SiO2/collagen: An efficient magnetic nanocatalyst for the synthesis of benzimidazole and benzothiazole derivatives

Ghafuri, Hossein,Esmaili, Elahe,Talebi, Majid

, p. 942 - 950 (2016/08/08)

In this project, Fe3O4@SiO2 was synthesized and combined with collagen for the preparation of Fe3O4@SiO2/collagen. It was characterized by FT-IR, 1H NMR, VSM, XRD, EDX, SEM and T

Peroxide-Free Pd(II)-Catalyzed Ortho Aroylation and Ortho Halogenation of Directing Arenes

Santra, Sourav Kumar,Banerjee, Arghya,Mohanta, Prakash Ranjan,Patel, Bhisma K.

, p. 6066 - 6074 (2016/07/26)

A Pd(II)-catalyzed peroxide-free ortho aroylation of directing arenes has been developed via cross dehydrogenative coupling (CDC) in the presence of the terminal oxidant Cu(OAc)2·H2O. Ortho aroylation of directing arenes proceeds via

Palladium catalyzed ortho-halogenation of 2-arylbenzothiazole and 2,3-diarylquinoxaline

Santra, Sourav Kumar,Banerjee, Arghya,Khatun, Nilufa,Samanta, Asim,Patel, Bhisma K.

, p. 11960 - 11965 (2015/02/19)

A palladium catalysed ortho-halogenation strategy has been developed using benzothiazoles and quinoxalines as the directing substrates. This method provides mono-o-halogenated product at the other available ortho site of a mono-ortho substituted 2-arylbenzothiazole. However, ortho-unsubstituted 2-arylbenzothiazole afforded di-ortho halogenated product exclusively. The preformed (or installed) ortho-group is towards the sulphur side of the benzothiazole from energy minimised calculation. Thus the selective formation of di-ortho-halogenated products is due to favourable exposure of the second ortho site for subsequent halogenation. However the phenyl ring in 2,3-diarylquinoxalines can be selectively mono ortho halogenated. A plausible reaction mechanism has been proposed for this halogenation process.

Samarium diiodide promoted reductive cyclization of nitrodisulfides with nitriles: A new route to benzothiazoles

Zhong,Zhang,Chen

, p. 316 - 318 (2007/10/03)

Benzothiazole derivatives are prepared via reductive cyclization of nitrodisulfides with nitriles promoted by SmI2 under mild and neutral conditions.

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