6054-00-8

Basic information

• Product Name: 3(2H)-isoflavene
• Synonyms: 3(2H)-isoflavene
• CAS NO: 6054-00-8
• Molecular Formula: C₁₅H₁₂O
• Molecular Weight: 208.26
• Mol File: 6054-00-8.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 340.5°C at 760 mmHg
• Flash Point: 156.3°C
• Appearance: /
• Density: 1.139g/cm³
• Vapor Pressure: 0.000169mmHg at 25°C
• Refractive Index: 1.618
• CAS DataBase Reference: 3(2H)-isoflavene(CAS DataBase Reference)
• NIST Chemistry Reference: 3(2H)-isoflavene(6054-00-8)
• EPA Substance Registry System: 3(2H)-isoflavene(6054-00-8)

Safety Data

• Hazardous Substances Data: 6054-00-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H12O/c1-2-6-12(7-3-1)14-10-13-8-4-5-9-15(13)16-11-14/h1-10H,11H2

Upstream product

• 254-04-6 2H-chromene 
• 591-50-4 iodobenzene 
• 82381-21-3 (E)-β-[2-hydroxyphenylethylene]benzeneethanol 
• 112635-45-7 C₁₅H₁₃BrO 
• 109790-41-2 [2-(2-oxo-2-phenylethoxy)benzyl]triphenylphosphonium bromide 
• 70340-04-4 (2-hydroxybenzyl)triphenylphosphonium bromide 
• 70-11-1 α-bromoacetophenone 
• 194665-78-6 2H-chromen-3-yl trifluoromethanesulfonate 
• 98-80-6 phenylboronic acid 
• 574-12-9 isoflavone 
• 90-01-7 salicylic alcohol 
• 109790-47-8 2-(o-hydroxymethylphenoxy)-1-phenylethanone 
• 3360-53-0 1-bromo-2-phenyl-1-propene 
• 112635-43-5 1,3-dibromo-2-phenylprop-1-ene 

Downstream Products

• 90878-07-2 2-(1-Ethyl-2-phenyl-allyl)-phenol 
• 4737-26-2 Isoflavan 
• 20879-06-5 (S)-3-phenylchromane 

Relevant articles and documents

Palladium-catalysed Intramolecular Arylation: a New Synthesis of Munduserone

Treatment of the aryl iodides (11) with palladium acetate gave the teracyclic stilbenes (13) via a formal but stereochemically disallowed Heck reaction; the method was exploited to synthesise (+/-)-munduserone (21).

Benzopyrans compound as well as preparation method and application thereof

The invention relates to the field of the agricultural fungicide, and specifically relates to a benzopyrans compound as well as a preparation method and application thereof. The benzopyrans compound provided by the invention is simple in structure, easy to synthesize, low in production cost, and has a good inhibiting effect on the strawberry botrytis cinerea, potato altemaria solani, and watermelon fusarium oxysporum.

FeCl3-Catalyzed Ring-Closing Carbonyl–Olefin Metathesis

Exploiting catalytic carbonyl–olefin metathesis is an ongoing challenge in organic synthesis. Reported herein is an FeCl3-catalyzed ring-closing carbonyl–olefin metathesis. The protocol allows access to a range of carbo-/heterocyclic alkenes wi