33714-13-5

Basic information

• Product Name: 3-indol-3-yl-3-(4-methoxy-phenyl)-1-p-tolyl-propan-1-one
• Synonyms: 3-indol-3-yl-3-(4-methoxy-phenyl)-1-p-tolyl-propan-1-one
• CAS NO: 33714-13-5
• Molecular Weight: 369.463
• Mol File: 33714-13-5.mol

Chemical Properties

• CAS DataBase Reference: 3-indol-3-yl-3-(4-methoxy-phenyl)-1-p-tolyl-propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-indol-3-yl-3-(4-methoxy-phenyl)-1-p-tolyl-propan-1-one(33714-13-5)
• EPA Substance Registry System: 3-indol-3-yl-3-(4-methoxy-phenyl)-1-p-tolyl-propan-1-one(33714-13-5)

Safety Data

• Hazardous Substances Data: 33714-13-5(Hazardous Substances Data)

Upstream product

• 120-72-9 indole 
• 6552-66-5 3-(4-methoxyphenyl)-1-p-tolylprop-2-en-1-one 
• 50990-40-4 (2E)-3-(4-methoxyphenyl)-1-(4-methylphenyl)prop-2-en-1-one 

Relevant articles and documents

The Michael Addition of Indole to α,β-Unsaturated Ketones Catalyzed by Iodine at Room Temperature

Indole undergoes conjugate addition with α,β-unsaturated ketones by means of alkylation of indole in the presence of a catalytic amount of molecular I2 at room temperature to afford the corresponding adduct in excellent yields (up to 96%). The

Catalytic conjugate addition of indole to α,β-unsaturated ketones by Co(ClO4)2·6H2O/bis-Schiff base complexes

Co(ClO4)2·6H2O/bis-Schiff base complexes promoted the conjugate addition of indole to α,β- unsaturated ketones under mild conditions, giving the corresponding addition products with high yields. And the complex has been ch

Ultrasound-accelerated Michael Addition of Indole to α,β- Unsaturated Ketones Catalyzed by Ceric Ammonium Nitrate (CAN)

Ceric ammonium nitrate efficiently catalyzes the Michael addition of indole to α,β-unsaturated carbonyl ketones by means of alkylation of indole under ultrasonic irradiation to afford the corresponding adduct in excellent yields. The substitution on the i