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4,6-Dimethyl-2(3H)-benzothiazolone, also known as DMABT, is a chemical compound with the molecular formula C9H9NO. It is a yellow crystalline solid that exhibits a sulfur-like odor. DMABT is widely recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as for its applications in various other industries.

80567-67-5

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80567-67-5 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
4,6-Dimethyl-2(3H)-benzothiazolone is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a key component in the development of new drugs and pesticides, contributing to advancements in healthcare and agriculture.
Used as a Fluorescent Indicator in Analytical Chemistry:
DMABT is utilized as a fluorescent indicator for the detection of sulfites and other sulfur-containing compounds in aqueous solutions. Its ability to fluoresce under specific conditions makes it a valuable tool for researchers and analysts in detecting and quantifying these compounds in various samples.
Used as a Chemical Reagent in Organic Synthesis:
In the field of organic synthesis, 4,6-Dimethyl-2(3H)-benzothiazolone serves as a chemical reagent. Its reactivity and stability make it suitable for use in a range of organic reactions, facilitating the synthesis of complex organic molecules.
Used in the Production of Dyes and Pigments:
DMABT is employed as a building block in the production of dyes and pigments. Its chemical properties allow it to contribute to the color and stability of these products, making it an important component in the manufacturing process.
Used in the Manufacturing of Rubber and Plastics:
In the rubber and plastics industry, 4,6-Dimethyl-2(3H)-benzothiazolone is used to enhance the properties of these materials. Its incorporation into rubber and plastic formulations can improve characteristics such as durability, flexibility, and resistance to various environmental factors.

Check Digit Verification of cas no

The CAS Registry Mumber 80567-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80567-67:
(7*8)+(6*0)+(5*5)+(4*6)+(3*7)+(2*6)+(1*7)=145
145 % 10 = 5
So 80567-67-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NOS/c1-5-3-6(2)8-7(4-5)12-9(11)10-8/h3-4H,1-2H3,(H,10,11)

80567-67-5SDS

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 4,6-dimethyl-3H-1,3-benzothiazol-2-one

1.2 Other means of identification

Product number -
Other names 4,6-Dimethyl-2(3H)-benzothiazolone

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:80567-67-5 SDS

80567-67-5Downstream Products

80567-67-5Relevant academic research and scientific papers

CuI-catalyzed one-pot synthesis of benzothiazolones from 2-iodoanilines-derived carbamates and sodium sulfide

Li, Jiaojiao,Zhang, Yihua,Jiang, Yongwen,Ma, Dawei

supporting information; experimental part, p. 2511 - 2513 (2012/06/16)

A copper-catalyzed procedure was developed for assembling benzothiazolones from ethyl 2-iodophenylcarbamates and sodium sulfide. A number of functional groups, such as methoxy, acyl, amide, carboxylate, trifluoromethyl, fluoro, and chloro, were tolerated under these conditions, providing benzothiazolones in good yields.

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