43100-26-1

Basic information

• Product Name: N,N'-bis(p-hydroxybenzoyl)hydrazine
• Synonyms: N,N'-bis(p-hydroxybenzoyl)hydrazine
• CAS NO: 43100-26-1
• Molecular Weight: 272.26
• Mol File: 43100-26-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N,N'-bis(p-hydroxybenzoyl)hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-bis(p-hydroxybenzoyl)hydrazine(43100-26-1)
• EPA Substance Registry System: N,N'-bis(p-hydroxybenzoyl)hydrazine(43100-26-1)

Safety Data

• Hazardous Substances Data: 43100-26-1(Hazardous Substances Data)

Upstream product

• 99-96-7 4-hydroxy-benzoic acid 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 5351-23-5 4-hydroxybenzoic acid hydrazide 
• 127-65-1 chloroamine-T 

Downstream Products

• 21022-23-1 N,N'-bis-(4-acetoxy-phenyl)-oxalamide 
• 10600-83-6 2,5-bis-(4-hydroxyphenyl)-1,3,4-oxadiazole 
• 21022-20-8 N,N'-Bis-(4-allyloxy-phenyl)-oxalamide 
• 19532-76-4 N,N'-bis(4-octyloxyphenyl)oxamide 

Relevant articles and documents

Synthesis of acylhydrazines and, symmetrical and asymmetrical diacylhydrazines from carboxylic acid via the Vilsmeier reagent mediated process

(Chloromethylene)dimethylammonium chloride (Vilsmeier reagent) has been used as an efficient and convenient reagent for the one-pot synthesis of acylhydrazines and symmetrical and asymmetrical diacylhydrazines from carboxylic acids. This reaction proceeded smoothly under mild conditions and it is quite practical, since the starting carboxylic acids can be easily handled and stored. Cleanliness, simplicity of the method and good to excellent yield of products are other advantages of this method.

Microwave-induced conversion of acid hydrazides to N,N′- diacylhydrazines in solvent-free conditions

A new and efficient method of converting acid hydrazides 1 to the corresponding N,N′-diacylhydrazines 2 under microwave irradiation and in solvent-free conditions has been described. Copyright Taylor & Francis Group, LLC.

Oxidation of Hydrazides Using Sodium Perborate: Formation of N,N′-Diacylhydrazines

Substituted aromatic hydrazides react very smoothly with sodium perborate in glacial acetic acid at room temperature to give N,N′-diacylhydrazines in excellent yields and purity.