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4505-48-0

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4505-48-0 Usage

Synthesis Reference(s)

Synthetic Communications, 15, p. 535, 1985 DOI: 10.1080/00397918508063838

Check Digit Verification of cas no

The CAS Registry Mumber 4505-48-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,0 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4505-48:
(6*4)+(5*5)+(4*0)+(3*5)+(2*4)+(1*8)=80
80 % 10 = 0
So 4505-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H12/c1-2-6-12(7-3-1)15-10-13-8-4-5-9-14(13)11-15/h1-10H,11H2

4505-48-0 Well-known Company Product Price

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  • Aldrich

  • (446300)  2-Phenylindene  97%

  • 4505-48-0

  • 446300-5G

  • 2,685.15CNY

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4505-48-0Relevant articles and documents

Supported palladium nanoparticle-catalysed Suzuki–Miyaura cross-coupling approach for synthesis of aminoarylbenzosuberene analogues from natural precursor

Bharti, Richa,Bal Reddy,Kumar, Sandeep,Das, Pralay

, (2017)

A semi-synthetic method has been developed for the synthesis of aminoarylbenzosuberenes (AABs) from naturally occurring himachalenes, an isomeric mixture of sesquiterpenes present in Cedrus deodara oil. Polymer-stabilized Pd(0) nanoparticle-catalysed Suzu

Bathocuproine-Enabled Nickel-Catalyzed Selective Ullmann Cross-Coupling of Two sp 2-Hybridized Organohalides

Li, Yuqiang,Yin, Guoyin

supporting information, p. 1657 - 1661 (2021/09/13)

Cross-coupling reactions are essential for the synthesis of complex organic molecules. Here, we report a nickel-catalyzed Ullmann cross-coupling of two sp 2-hybridized organohalides, featuring high cross-selectivity when the two coupling partners are used in a 1:1 ratio. The high chemoselectivity is governed by the bathocuproine ligand. Moreover, the mild reductive reaction conditions allow that a wide range of functional groups are compatible in this Ullmann cross-coupling.

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

supporting information, p. 10566 - 10573 (2020/04/15)

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

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