1019777-27-5

Basic information

• Product Name: pent-4-en-1-yl 2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetate
• Synonyms: pent-4-en-1-yl 2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetate
• CAS NO: 1019777-27-5
• Molecular Weight: 425.912
• Mol File: 1019777-27-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: pent-4-en-1-yl 2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: pent-4-en-1-yl 2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetate(1019777-27-5)
• EPA Substance Registry System: pent-4-en-1-yl 2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetate(1019777-27-5)

Safety Data

• Hazardous Substances Data: 1019777-27-5(Hazardous Substances Data)

Upstream product

• 821-09-0 n-Pent-4-enyl alcohol 
• 53-86-1 [1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetic acid 

Downstream Products

• 1019777-24-2 1-(4-(4'-methoxyphenyl)benzoyl)-5-methoxy-2-methylindole-3-acetic acid 4-pentenyl ester 
• 1574209-53-2 pent-4-en-1-yl 2-(5-methoxy-2-methyl-1(4-(piperidine-1-carboxamido)benzoyl)-1H-indol-3-yl)acetate 

Relevant articles and documents

Redox-Neutral Nickel(II) Catalysis: Hydroarylation of Unactivated Alkenes with Arylboronic Acids

Reported here is the discovery of a redox-neutral NiII/NiII catalytic cycle which is capable of the linear-selective hydroarylation of unactivated alkenes with arylboronic acids for the first time. This novel catalytic cycle, enabled

Installation of protected ammonia equivalents onto aromatic & heteroaromatic rings in water enabled by micellar catalysis

A single set of conditions consisting of a palladium catalyst, a commercially available ligand, and a base, allow for several types of C-N bond constructions to be conducted in water with the aid of a commercially available "designer" surfactant (TPGS-750-M). Products containing a protected NH2 group in the form of a carbamate, sulfonamide, or urea can be fashioned starting with aryl or heteroaryl bromides, iodides, and in some cases, chlorides, as substrates. Reaction temperatures are in the range of room temperature to, at most, 50 °C, and result in essentially full conversion and good isolated yields.