38901-87-0

Basic information

• Product Name: 2,5-Cyclohexadiene-1,4-dione, mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone]
• CAS NO: 38901-87-0
• Molecular Formula: C14H11N3OS
• Molecular Weight: 269.327
• Mol File: 38901-87-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,5-Cyclohexadiene-1,4-dione, mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone](CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Cyclohexadiene-1,4-dione, mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone](38901-87-0)
• EPA Substance Registry System: 2,5-Cyclohexadiene-1,4-dione, mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone](38901-87-0)

Safety Data

• Hazardous Substances Data: 38901-87-0(Hazardous Substances Data)

Usage

General Description

2,5-Cyclohexadiene-1,4-dione, mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone] is a chemical compound that is derived from both cyclohexadiene-1,4-dione and 3-methyl-2(3H)-benzothiazolylidene hydrazone. It is used in various chemical and pharmaceutical applications due to its unique properties and reactivity. The compound is commonly used as a reagent or intermediate in organic synthesis and is also being researched for its potential medicinal properties. Due to its complex structure and reactivity, 2,5-Cyclohexadiene-1,4-dione, mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone] requires careful handling and storage to ensure its stability and effectiveness in various applications.

Upstream product

• 112900-64-8 2-<4-N-methyl-N-<2-(4-nitrophenoxy)ethyl>aminophenylazo>-3-methylbenzothiazolium chloride 
• 20064-89-5 2-(4-dimethylamino-phenylazo)-3-methyl-benzothiazolium; iodide 
• 10335-52-1 4-benzothiazole-2-ylazophenol 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 
• 1128-67-2 3-methyl-2-benzothiazolinone hydrazone 
• 108-95-2 phenol 
• 106-51-4 p-benzoquinone 

Downstream Products

• 65902-55-8 2-(4-methoxy-phenylazo)-benzothiazole 

Relevant articles and documents

Automated colorimetric microdetermination of phenols by oxidative coupling with 3-methyl-2-benzothiazolinone hydrazone.

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NUCLEOPHILIC AROMATIC SUBSTITUTION: FADING OF BENZOTHIAZOLIUM AZO DYES IN ALKALINE SOLUTION

Benzothiazolium azo dyes bearing a 4'-amino function hydrolyse in alkali according to the equation:.The reaction is catalysed by amines; a dye with R1=CH2CH2OH exhibits a third-order kinetic term (k3->) which is not observed with dyes without a hydroxyl group in R1 or R2.Methoxide ion gives reversible formation of a ?-bonded adduct with the dyes; benzothiazolium azo dyes with weakly basic amine substituents react with hydroxide ion to form adducts which regenerate the azo dye on addition of acid.