1193731-90-6

Basic information

• Product Name: (E)-N'-(2-hydroxy-6-methoxylbenzylidene)acetohydrazide
• Synonyms: (E)-N'-(2-hydroxy-6-methoxylbenzylidene)acetohydrazide
• CAS NO: 1193731-90-6
• Molecular Weight: 208.217
• Mol File: 1193731-90-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-N'-(2-hydroxy-6-methoxylbenzylidene)acetohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N'-(2-hydroxy-6-methoxylbenzylidene)acetohydrazide(1193731-90-6)
• EPA Substance Registry System: (E)-N'-(2-hydroxy-6-methoxylbenzylidene)acetohydrazide(1193731-90-6)

Safety Data

• Hazardous Substances Data: 1193731-90-6(Hazardous Substances Data)

Upstream product

• 700-44-7 6-methoxysalicylaldehyde 
• 1068-57-1 acetic acid hydrazide 

Downstream Products

• 1193731-71-3 2-acetyl-6-methoxybenzaldehyde 

Relevant articles and documents

Phthalides by rhodium-catalyzed ketone hydroacylation

(Chemical Equation Presented) Phthalides are biologically relevant five-membered lactones found in herbs, fruits, and vegetables. Herein we communicate the first atom-economical approach to phthalides by using enantioselective ketone hydroacylation. In the presence of Rh[(Duanphos)]X (X = NO3, OTf, OMs), various 2-ketobenzaldehydes undergo intramolecular hydroacylation to produce phthalide products in good yields and 92-98% ee's. Our study highlights the key role counterions play in controlling both reactivity and enantioselectivity. A concise asymmetric total synthesis of the celery extract (S)-(-)-3-n-butylphthalide is also presented.