39246-00-9

Basic information

• Product Name: p-phenylenediacetaldehyde
• Synonyms: p-phenylenediacetaldehyde
• CAS NO: 39246-00-9
• Molecular Weight: 162.188
• Mol File: 39246-00-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: p-phenylenediacetaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: p-phenylenediacetaldehyde(39246-00-9)
• EPA Substance Registry System: p-phenylenediacetaldehyde(39246-00-9)

Safety Data

• Hazardous Substances Data: 39246-00-9(Hazardous Substances Data)

Upstream product

• 2664-28-0 1,4-diallylbenzene 
• 36076-26-3 diethyl 2,2'-(1,4-phenylene)diacetate 
• 7325-46-4 1,4-phenylenediacetic acid 
• 5140-03-4 2-[4-(2-hydroxyethyl)phenyl]ethan-1-ol 
• 39245-97-1 3,5,3',5'-tetramethyl-1H,1'H-1,1'-(p-phenylene-diacetyl)-bis-pyrazole 
• 43213-57-6 2,2'-p-phenylenedimethyl-bis-[1,3]dioxolane 

Downstream Products

• 5140-03-4 2-[4-(2-hydroxyethyl)phenyl]ethan-1-ol 
• 41791-00-8 4,5-diphenylphenanthrene 
• 874338-61-1 1-phenyl-4-[4-(2-hydroxy-4-phenyl-3-butynyl)phenyl]but-3-yn-2-ol 

Relevant articles and documents

Method for preparing dialdehyde compound by using dicarboxylic acid

The invention relates to the technical field of chemical synthesis, and particularly relates to a method for preparing a dialdehyde compound by using dicarboxylic acid. The method disclosed by the invention comprises the following step that under the cata

Synthesis of naphthalenes and 2-naphthols by the electrophilic cyclization of alkynes

A wide variety of substituted naphthalenes are readily prepared regioselectively under mild reaction conditions by the 6-endo-dig electrophilic cyclization of appropriate arene-containing propargylic alcohols by IC1, I 2, Br2, NBS, and PhSeBr. 3-Iodo-2-naphthols have also been prepared in excellent yields by the cyclization of analogous 1-aryl-3-alkyn-2-ones. This methodology readily accommodates various functional groups and has been successfully extended to the synthesis of substituted carbazoles and dibenzothiophenes.