2814-60-0

Basic information

• Product Name: (2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole
• CAS NO: 2814-60-0
• Molecular Formula: C₁₈H₁₈N₄S₂
• Molecular Weight: 354.4923
• Mol File: 2814-60-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 528.7°C at 760 mmHg
• Flash Point: 273.5°C
• Density: 1.32g/cm³
• Vapor Pressure: 2.9E-11mmHg at 25°C
• Refractive Index: 1.713
• CAS DataBase Reference: (2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole(CAS DataBase Reference)
• NIST Chemistry Reference: (2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole(2814-60-0)
• EPA Substance Registry System: (2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole(2814-60-0)

Safety Data

• Hazardous Substances Data: 2814-60-0(Hazardous Substances Data)

Usage

Description

(2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole is a complex organic compound with a molecular formula of C17H19N3S2. It features a benzothiazole ring, an ethyl group, and a hydrazono group attached to the benzothiazole ring. (2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole has potential applications in various fields, including pharmaceuticals, agriculture, and materials science. However, due to its complex structure and potentially reactive hydrazono group, careful handling and further research are required to fully understand its properties and potential uses.

Uses

Used in Pharmaceutical Industry:
(2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole is used as a pharmaceutical compound for its potential therapeutic properties. Its complex structure and the presence of a hydrazono group may contribute to its interaction with biological targets, making it a candidate for drug development.
Used in Agriculture:
In the agricultural industry, (2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole may be utilized as a pesticide or a component in fertilizers. Its complex structure could potentially offer new modes of action against pests or enhance crop growth and yield.
Used in Materials Science:
(2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole can be employed in materials science for the development of new materials with unique properties. The benzothiazole ring and hydrazono group may contribute to the compound's stability, reactivity, or other characteristics that could be beneficial in creating advanced materials for various applications.

Upstream product

• 615-22-5 2-methylmercaptobenzothiazole 
• 80-40-0 ethyl ester of p-toluenesulfonic acid 
• 28218-93-1 3-ethyl-2-benzothiazolinone hydrazone 
• 19617-05-1 (3-ethyl-3H-benzothiazol-2-ylidene)-nitroso-amine 
• 5773-04-6 3,3'-diethyl-2,3,2',3'-tetrahydro-2,2'-(1Z,2E,4Z)-tetrazenediylidene-bis-benzothiazole 
• 87515-67-1 2-ethylthio-3-ethylbenzothiazolinium iodide 
• 78485-28-6 azido-(3-ethyl-3H-benzothiazol-2-ylidene)-amine 
• 103-69-5 N-ethyl-N-phenylamine 
• 3955-58-6 N-ethyl-N-phenylthiourea 
• 934-34-9 2-hydroxybenzothiazole 
• 74-96-4 ethyl bromide 
• 6468-14-0 3-ethyl-2-benzothiazolinone 
• 137-07-5 2-amino-benzenethiol 
• 95-55-6 2-amino-phenol 

Relevant articles and documents

Excited state electronic structures and photochemistry of different oxidation states of 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS)

The molecular structures of 2,2-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), were calculated by using time-dependent density functional theory (TDDFT) model with M062X method with 6-311G (d, p) basis set. In this work, the ABTS were theoreti

Preparation method of 2, 2'-azino-bis(3-alkylbenzothiazoline-6-sulfonic acid) salt

The invention discloses a preparation method of a 2, 2'-azino-bis(3-alkylbenzothiazoline-6-sulfonic acid) salt. The raw materials used in the preparation method are easily available, and the price islow, the production cost can be greatly reduced while ensuring a high reaction yield, so that enlarged production is facilitated, meanwhile, the preparation method is different from the previous new preparation process, and the new preparation process is beneficial to academic research, industrial research and practice of ABTS in the field, so that the development of related technologies and related industrial economy in the field is promoted.

Method for synthesizing 2,2'-diamine-bis(3-ethylbenzothiazoline-6- sulfoacid)diamine salt

The invention provides a method for synthesizing 2,2'-diamine-bis(3-ethylbenzothiazoline-6-sulfoacid)diamine salt(ABTS), which belongs to the field of organic synthesis. According to the invention, 2-hydroxybenzothiazole is reacted with 2-ethyl bromide to form 3-ethylbenzothiazole-2-ketone, and then is reacted with hydrazine hydrate to generate 2,2'-azino-bis(3-ethylbenzothiazoline), 2,2'-azino-bis(3-ethylbenzothiazoline) is subjected to a sulfonation reaction with concentrated sulfuric acid to generate a compound 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfoacid), and finally the compound isreacted with ammonia gas to generate 2,2'-diamine-bis(3-ethylbenzothiazoline-6-sulfoacid)diamine salt. The raw materials used in the invention are cheap and easy to obtain, the operation is simple andconvenient, the reaction conditions are mild, and the yield is high.