177496-78-5

Basic information

• Product Name: 2-acetoxy-5-nitrobenzaldehyde
• Synonyms: 2-acetoxy-5-nitrobenzaldehyde
• CAS NO: 177496-78-5
• Molecular Weight: 209.158
• Mol File: 177496-78-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-acetoxy-5-nitrobenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-acetoxy-5-nitrobenzaldehyde(177496-78-5)
• EPA Substance Registry System: 2-acetoxy-5-nitrobenzaldehyde(177496-78-5)

Safety Data

• Hazardous Substances Data: 177496-78-5(Hazardous Substances Data)

Upstream product

• 97-51-8 5-Nitrosalicylaldehyde 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 
• 24590-01-0 acetyloxy(2-acetyloxy-5-nitrophenyl)methyl acetate 

Downstream Products

• 2725-81-7 6-nitrocoumarin 
• 197314-77-5 5-nitro-2-hydroxy-(E)-cinnamic acid methyl ester 

Relevant articles and documents

Bismuth (III) chlorides; an efficient and selective catalyst for deprotection of 1,1-diacetates

A variety of 1,1-diacetates are easily and efficiently deprotected in the presence of catalytic amounts of bismuth(III) chloride affording the corresponding aldehydes in high yields.

Copper(I)-catalyzed hydroalkoxylation/hydrogen-bonding-induced asymmetric hetero-diels-alder cycloaddition cascade: An approach to aromatic spiroketals

One thing leads to another: Bis(benzannelated) 5,6-spiroketal skeletons can be constructed by an efficient cascade process involving an unprecedented CuI-catalyzed intramolecular alkyne hydroalkoxylation and an asymmetric hetero-Diels-Alder cyc

Efficient and selective deprotection of aryl aldehyde diacetates catalyzed by tin(II) chloride dihydrate

A mild, efficient and excellent yield method for the selective deprotection of aryl aldehyde diacetates in the presence of phenolic acetate and aliphatic aldehyde diacetate using catalytic amounts of tin(II) chloride dihydrate (SnCl2.2H2O) is described.