4114-25-4

Basic information

• Product Name: 1,3-bis(benzylideneamino)urea
• Synonyms: 1,3-bis(benzylideneamino)urea
• CAS NO: 4114-25-4
• Molecular Formula: C₁₅H₁₄N₄O
• Molecular Weight: 0
• Mol File: 4114-25-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.14g/cm³
• CAS DataBase Reference: 1,3-bis(benzylideneamino)urea(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-bis(benzylideneamino)urea(4114-25-4)
• EPA Substance Registry System: 1,3-bis(benzylideneamino)urea(4114-25-4)

Safety Data

• Hazardous Substances Data: 4114-25-4(Hazardous Substances Data)

Usage

General Description

1,3-bis(benzylideneamino)urea, also known as DBAU, is a chemical compound that belongs to the class of urea derivatives. It is often used as a ligand in coordination chemistry and has been studied for its potential antitumor and anti-inflammatory properties. DBAU has a unique molecular structure with two benzylideneamino groups attached to the urea backbone. 1,3-bis(benzylideneamino)urea has shown promising results in inhibiting the growth of cancer cells and reducing inflammation in various preclinical studies. Its potential applications in the fields of medicinal chemistry and drug development make it an interesting molecule for further research and exploration.

Upstream product

• 497-18-7 carbonodihydrazide 
• 100-52-7 benzaldehyde 
• 7732-18-5 water 
• 584-08-7 potassium carbonate 
• 94521-03-6 1-(diethoxyphosphoryl)-2-(phenylmethylidene)hydrazine 
• 1666-17-7 benzaldehyde p-toluenesulfonylhydrazone 

Downstream Products

• 1617-16-9 hydrazine-N,N'-dicarboxylic acid bis-benzylidenehydrazide 
• 28867-76-7 benzaldehyde benzylidenehydrazone 
• 21531-96-4 4-aminourazole 
• 70249-89-7 4-benzylideneamino-5-phenyl-2,4-dihydro-[1,2,4]triazol-3-one 
• 139355-70-7 2,4-dibenzylidenamino-1,2,4-thiadiazolidine-3,5-dione 
• 137678-64-9 1,3-bis(benzylideneamino)-2,4-imidazolidinedione 
• 100-52-7 benzaldehyde 
• 57735-10-1 4-amino-5-phenyl-2,4-dihydro-[1,2,4]triazol-3-one 
• 262291-22-5 La(C₁₅H₁₄N₄O)Cl₃ 
• 262291-27-0 Pr(C₁₅H₁₄N₄O)Cl₃ 
• 1361230-70-7 carbo-di(N'-benzylidene-N-ethylhydrazide) 
• 1361230-77-4 carbo-N'-benzylidene-N-benzylhydrazide(N'-benzylidene-N-ethylhydrazide) 
• 1361230-89-8 2-benzyl-4-ethyl-6-phenyl-1,2,4,5-tetrazinan-3-one 
• 1361230-90-1 2-methyl-6-phenyl-4-propyl-1,2,4,5-tetrazinan-3-one 

Relevant articles and documents

Olive-Shaped Organic Cages: Synthesis and Remarkable Promotion of Hydrazone Condensation through Encapsulation in Water

Two organic cages have been prepared in situ in water through the 2 + 3 hydrazone coupling of two pyridinium-derived trialdehydes and oxalohydrazide. The highly water-soluble cages encapsulate and solubilize linear neutral molecules. Such encapsulation ha

Efficient synthesis of 1,5-disubstituted carbohydrazones using K 2CO3 as a carbonyl donor

A novel reaction that generates 1,5-disubstituted carbohydrazones via the carbonylation of tosylhydrazones has been developed. For the first time, the inexpensive, readily available, environmentally friendly, and nongaseous potassium carbonate is used as

Synthesis, spectroscopic characterization and invitro antimicrobial investigation of some Hg(II) complex of carbohydrazone

The synthesis of novel mercury (II) complex with new ligands derived from Carbohydrazides has been reported. The complexes have general composition [HgL2X2], Where L= Carbohydrazone and X = Cl-, NO3-.