Cas 20904-82-9,2-([1,1'-biphenyl]-4-yl)-1H-indene

20904-82-9

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Basic information

Product Name: 2-([1,1'-biphenyl]-4-yl)-1H-indene
Synonyms: 2-([1,1'-biphenyl]-4-yl)-1H-indene
CAS NO:20904-82-9
Molecular Formula:
Molecular Weight: 268.358
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-([1,1'-biphenyl]-4-yl)-1H-indene(CAS DataBase Reference)
NIST Chemistry Reference: 2-([1,1'-biphenyl]-4-yl)-1H-indene(20904-82-9)
EPA Substance Registry System: 2-([1,1'-biphenyl]-4-yl)-1H-indene(20904-82-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 20904-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 20904-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,0 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20904-82:
(7*2)+(6*0)+(5*9)+(4*0)+(3*4)+(2*8)+(1*2)=89
89 % 10 = 9
So 20904-82-9 is a valid CAS Registry Number.

20904-82-9Upstream product

20904-82-9Downstream Products

20904-82-9Relevant academic research and scientific papers

Bridged Stilbenes: AIEgens Designed via a Simple Strategy to Control the Non-radiative Decay Pathway

Igawa, Kazunobu,Iwai, Riki,Konishi, Gen-ichi,Morokuma, Keiji,Sairi, Amir Sharidan,Sasaki, Shunsuke,Suenobu, Tomoyoshi,Suzuki, Satoshi

, p. 10566 - 10573 (2020)

To broaden the application of aggregation-induced emission (AIE) luminogens (AIEgens), the design of novel small-molecular dyes that exhibit high fluorescence quantum yield (Φfl) in the solid state is required. Considering that the mechanism of

Process for preparing 2-aryl-substituted indenes

-

, (2008/06/13)

A process is disclosed for preparing 2-aryl-substituted indenes by reacting an indene with an arene compound substituted with an halogen atom, preferably a iodine atom, or with an organosulphonate group, said reaction being carried out in a basic medium i

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