4080-88-0

Basic information

• Product Name: DIPHENYLAZELATE
• Synonyms: DIPHENYLAZELATE;AZELAICACID,DIPHENYLESTER
• CAS NO: 4080-88-0
• Molecular Formula: C₂₁H₂₄O₄
• Molecular Weight: 340.41
• Mol File: 4080-88-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DIPHENYLAZELATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIPHENYLAZELATE(4080-88-0)
• EPA Substance Registry System: DIPHENYLAZELATE(4080-88-0)

Safety Data

• Hazardous Substances Data: 4080-88-0(Hazardous Substances Data)

Upstream product

• 123-99-9 azelaic acid 
• 108-95-2 phenol 
• 123-98-8 azelaoyl chloride 
• 102-09-0 bis(phenyl) carbonate 

Relevant articles and documents

Doubly Strapped Redox-Switchable 5,10,15,20-Tetraaryl-5,15-diazaporphyrinoids: Promising Platforms for the Evaluation of Paratropic and Diatropic Ring-Current Effects

This paper presents a novel series of chemically stable and redox-switchable 20π, 19π, and 18π5,10,15,20-tetraaryl-5,15-diazaporphyrinoids (TADAPs) that have two alkyl-chain straps above and below the diazaporphyrin ring. Three types of doubly strapped TA

Base catalyzed sustainable synthesis of phenyl esters from carboxylic acids using diphenyl carbonate

Phenyl esters were obtained in moderate to high yields by reaction of aliphatic and aromatic carboxylic acids with one equivalent of diphenyl carbonate in the presence of catalytic amounts of tertiary amine bases, such as DBU, TBD and DMAP under neat conditions at elevated temperatures (>100°C).

Design and synthesis of calcium and magnesium ionophores based on double-armed diazacrown ether compounds and their application to an ion-sensing component for an ion-selective electrode

The double-armed diazacrown ethers, which have a base diazacrown ether ring with two diamide-type side chains, were designed and synthesized on the basis of the proposed molecular model for the novel neutral Ca2+ and Mg2+ ionophores. The potentiometric ion-selective electrodes were prepared with over 20 kinds of systematically synthesized diazacrown ether derivatives. The relationship between the molecular structures of the ionophores and the ion selectivities was fully discussed. The electrodes based on the 21- and 18-membered diazacrown ether derivatives possessing a glycolic diamide and malonic diamide in their side chains (K23E1 and K22B5) exhibited excellent Ca2+ and Mg2+ selectivities, respectively. The ion-selectivity features of the novel Ca2+ and Mg2+ ionophores supply important structural information about the design of host molecules for alkaline earth metal cations.