1262136-56-0

Basic information

• Product Name: C₃₈H₄₂N₄O₄
• CAS NO: 1262136-56-0
• Molecular Weight: 618.776
• Mol File: 1262136-56-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₈H₄₂N₄O₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₈H₄₂N₄O₄(1262136-56-0)
• EPA Substance Registry System: C₃₈H₄₂N₄O₄(1262136-56-0)

Safety Data

• Hazardous Substances Data: 1262136-56-0(Hazardous Substances Data)

Upstream product

• 99-93-4 4-Hydroxyacetophenone 
• 123-11-5 4-methoxy-benzaldehyde 
• 99174-33-1 1,1'-<1,6-hexanediylbis(oxy-4,1-phenylene)>bisethanone 
• 6338-81-4 (E)-1-(4-hydroxyphenyl)-3-(4-methoxyphenyl)-2-propen-1-one 
• 629-03-8 1 ,6-dibromohexane 

Relevant articles and documents

Syntheses and reactions of 4'-[(ω-bromoalkyl)oxy]-and 4',4'''-(polymethylenedoxy)-bis substituted chalcones

Base catalyzed condensation of 4-hydroxyacetophenone (1) with several aldehydes resulted 4'-hydroxychalcones (2a-c). Reaction of α,ω-dibromoalkanes (3, n=2, 4 & 6) with (2a-c) in equimolar ratio resulted a mixture of 4'-[(ω-bromoalkyl)oxy]- substituted chalcones (4a-i) and 4',4'''-(polymethylenedioxy)-bis substituted chalcones (5a-i) separated by ethanol as soluble (4a-i) and insoluble (5a-i) products. Compounds (5a-i) were also synthesized by another route. Compound 1 on treatment with 3 in molar ratio 2:1 resulted 4',4'''-(polymethylenedioxy)-diacetophenone (4#a-c) which on base catalyzed condensation gave compounds (5a-i). Reaction of 4d with substituted phenols and thiophenols gave corresponding phenoxy and thiophenoxy substituted chalcones (6a-f) where as compounds 5a, 5b, 5d, 5h and 5e on treatment with hydrazine hydrate furnished corresponding bis-2-pyrazolines (7a-e). The structures of all synthesized compounds were confirmed on the basis of analytical and spectral data.