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2,3-Dihydro-3-methyl-2-methylenebenzothiazoles are heterocyclic compounds that consist of a benzene ring fused to a thiazole ring. The thiazole ring contains a sulfur atom and a nitrogen atom, while the benzene ring is attached to a methyl group at the 3-position and a methylene group at the 2-position. These compounds are typically colorless or pale yellow crystalline solids with a characteristic odor.

23574-67-6

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23574-67-6 Usage

Uses

1. Corrosion Inhibitors: 2,3-Dihydro-3-methyl-2-methylenebenzothiazoles are used as corrosion inhibitors in various industrial applications, such as oil and gas pipelines, water treatment systems, and cooling systems. They help to prevent the formation of rust and other corrosion products, thereby extending the life of the equipment and reducing maintenance costs.
2. Antimicrobial Agents: These compounds exhibit antimicrobial properties and can be used as preservatives in various products, such as cosmetics, personal care products, and pharmaceuticals. They help to inhibit the growth of bacteria, fungi, and other microorganisms, ensuring the safety and shelf life of the products.
3. Rubber Industry: 2,3-Dihydro-3-methyl-2-methylenebenzothiazoles are used as accelerators in the rubber industry. They help to speed up the vulcanization process, which is the process of converting raw rubber into a more durable and elastic material. This results in improved rubber properties and reduced production time.
4. Dyes and Pigments: These compounds can be used as intermediates in the synthesis of dyes and pigments for various applications, such as textiles, plastics, and printing inks. They contribute to the color and stability of the final products.
5. Analytical Reagents: 2,3-Dihydro-3-methyl-2-methylenebenzothiazoles can be used as analytical reagents in various chemical analyses, such as spectrophotometry and chromatography. They help to improve the sensitivity and selectivity of the analytical methods.
6. Pharmaceutical Industry: These compounds can be used as intermediates in the synthesis of various pharmaceutical drugs. They may have potential applications in the development of new medications for the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 23574-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,7 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23574-67:
(7*2)+(6*3)+(5*5)+(4*7)+(3*4)+(2*6)+(1*7)=116
116 % 10 = 6
So 23574-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NS/c1-7-10(2)8-5-3-4-6-9(8)11-7/h3-6H,1H2,2H3

23574-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2-methylidene-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names benzothiazole

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:23574-67-6 SDS

23574-67-6Relevant academic research and scientific papers

THERMOLYSIS OF QUARTENARY SALTS OF 2-METHYLBENZOTHIAZOLE AND THEIR METHYLENE BASES

Al'perovich, M. A.,Khesin, V. G.,Raikhina, R. D.,Medvedeva, T. D.

, p. 1182 - 1187 (2007/10/02)

The pathways of the thermal transformations of quartenary salts of 2-methylbenzothiazole and their methylene bases were investigated.The schemes of the thermal fragmentation of these compounds are discussed.The possibility of the formation of methylene bases in the thermolysis of quartenary salts of 2-methylbenzothiazole is demonstrated.

INVESTIGATION OF THE PATHWAYS OF THERMAL FRAGMENTATION OF THIACARBOCYANINE DYES

Khesin, V. G.,Al'perovich, M. A.,Abramenko, P. I.

, p. 1187 - 1192 (2007/10/02)

The pathways of the thermal transformations of thiacarbocyanines with various alkyl groups attached to the ring nitrogen atoms of the heteroresidues, of 3,3'-diethylthiacarbocyanine with various anions, and its anhydro base were investigated.The results of the studies are compared with the results of quantum-chemical calculations of the labilities of the bonds in these compounds by the Pariser-Parr-Pople method.

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