168649-23-8

Basic information

• Product Name: 1H-Indole-3-acetic acid, 5-phenyl-
• Synonyms: 1H-Indole-3-acetic acid,5-phenyl
• CAS NO: 168649-23-8
• Molecular Formula: C16H13NO2
• Molecular Weight: 251.28000
• Mol File: 168649-23-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 521.3±35.0 °C(Predicted)
• Density: 1.291±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1H-Indole-3-acetic acid, 5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-3-acetic acid, 5-phenyl-(168649-23-8)
• EPA Substance Registry System: 1H-Indole-3-acetic acid, 5-phenyl-(168649-23-8)

Safety Data

• Hazardous Substances Data: 168649-23-8(Hazardous Substances Data)

Usage

Chemical class

Indole-3-acetic acid derivatives

Common use

Plant growth regulator

Function

Promotes growth and development of plants

Activity

Auxin-like

Agricultural and horticultural applications

Enhances root development, flowering, and fruiting in various plant species

Potential role

Promoting stress tolerance and improving crop yield

Significance

Important in the agricultural industry and plant science research.

Upstream product

• 1124-19-2 phenyltin trichloride 
• 40432-84-6 (5-bromo-1H-indol-3-yl)-acetic acid 
• 66616-72-6 5-phenyl-1H-indole 

Relevant articles and documents

PLANT GROWTH REGULATOR

Providing an auxin derivative that can exert its intended effect more efficiently, while reducing any unintended effects. A compound represented by the General Formula (1) having a specific substituent at the 5- and/or 6-position of the auxin indole ring.

Palladium-Catalyzed Stille Couplings of Aryl, Vinyl-, and Alkyltrichlorostannanes in Aqueous Solution

Stille Coupling of water-soluble aryl and vinyl halides with alkyl, aryl-, and vinyltrichlorostannane derivatives (RSnCl3) are effected in aqueous solution using a catalyst generated in situ from PdCl2 and KOH both with and without added PhP(mC6H4SO3Na)2.The yields are generally good to excellent, although some limitations of the protocol are described.