51086-08-9

Basic information

• Product Name: 5-(allyloxy)-1H-indole
• Synonyms: 5-(allyloxy)-1H-indole;5-(2-propen-1-yloxy)-1H-Indole
• CAS NO: 51086-08-9
• Molecular Formula: C₁₁H₁₁NO
• Molecular Weight: 173.21114
• Mol File: 51086-08-9.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 332.661°C at 760 mmHg
• Flash Point: 121.777°C
• Appearance: /
• Density: 1.125g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.622
• PKA: 16.78±0.30(Predicted)
• CAS DataBase Reference: 5-(allyloxy)-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(allyloxy)-1H-indole(51086-08-9)
• EPA Substance Registry System: 5-(allyloxy)-1H-indole(51086-08-9)

Safety Data

• Hazardous Substances Data: 51086-08-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H11NO/c1-2-7-13-10-3-4-11-9(8-10)5-6-12-11/h2-6,8,12H,1,7H2

Upstream product

• 1953-54-4 indol-5-ol 
• 106-95-6 allyl bromide 
• 2581-34-2 3-methyl-4-nitrophenol 
• 120106-18-5 4-(allyloxy)-2-methyl-1-nitrobenzene 
• 556-56-9 allyl iodid 

Downstream Products

• 132560-36-2 4-allyl-1-benzoyl-5-methoxy-2,3-dihydroindole 
• 132560-37-3 1-benzoyl-5-methoxy-2,3-dihydroindole-4-acetaldehyde 
• 132560-38-4 1-benzoyl-4-(2'-di-n-propylaminoethyl)-5-methoxy-2,3-dihydroindole 
• 1092837-34-7 5-(allyloxy)-1-tosyl-1H-indole 
• 1386456-34-3 5-allyloxy-1H-indole-3-carbaldehyde 
• 710982-56-2 5-allyloxy-1-benzenesulfonyl-1H-indole 

Relevant articles and documents

Synthesis of a dihydropyrano[3,2-e]indole as a rotationally restricted phenolic analog of the neurotransmitter serotonin

1-(2-Dimethylaminoethyl)-8,9-dihydropyrano[3,2-e]indole has been synthesized via a six step procedure involving a Claisen rearrangement of a 5-allyloxyindole-3-glyoxamide. This novel heterocycle (1) represents a rotationally restricted phenolic analog of the neurotransmitter [3-(2-aminoethyl)-5-hydroxyindole].

Total synthesis of (-)-serotobenine

The efficient total synthesis of (?)-serotobenine (1) has been achieved by constructing an optically active dihydrobenzofuran ring via a rhodium carbenoid mediated intramolecular C?H insertion reaction, which was developed by our group. Then the possibili

Antidiabetic agents

The instant invention is concerned with aryl and heteroaryl oxyacetic acid type compounds which are useful antidiabetic compounds. Compositions and methods for the use of the compounds in the treatment of diabetes and related diseases and for lowering triglyceride levels are also disclosed.