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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

Alumina-Mediated π-Activation of Alkynes

Akhmetov, Vladimir,Amsharov, Konstantin,Feofanov, Mikhail,Sharapa, Dmitry I.

, p. 15420 - 15426 (2021/09/30)

The ability to induce powerful atom-economic transformation of alkynes is the key feature of carbophilic π-Lewis acids such as gold- and platinum-based catalysts. The unique catalytic activity of these compounds in electrophilic activations of alkynes is explained through relativistic effects, enabling efficient orbital overlapping with π-systems. For this reason, it is believed that noble metals are indispensable components in the catalysis of such reactions. In this study, we report that thermally activated γ-Al2O3activates enynes, diynes, and arene-ynes in a manner enabling reactions that were typically assigned to the softest π-Lewis acids, while some were known to be triggered exclusively by gold catalysts. We demonstrate the scope of these transformations and suggest a qualitative explanation of this phenomenon based on the Dewar-Chatt-Duncanson model confirmed by density functional theory calculations.

Small Gold(I) and Gold(I)–Silver(I) Clusters by C?Si Auration

Pei, Xiao-Li,Pereira, Ana,Smirnova, Ekaterina S.,Echavarren, Antonio M.

supporting information, p. 7309 - 7313 (2020/05/18)

Auration of o-trimethylsilyl arylphosphines leads to the formation of gold and gold–silver clusters with ortho-metalated phosphines displaying 3c–2e Au?C?M bonds (M=Au/Ag). Hexagold clusters [Au6L4](X)2 are obtained by reaction of (L?TMS)AuCl with AgX, whereas reaction with AgX and Ag2O leads to gold–silver clusters [Au4Ag2L4](X)2. Oxo-trigold(I) species [Au3O]+ were identified as the intermediates in the formation of the silver-doped clusters. Other [Au5], [Au4Ag], and [Au12Ag4] clusters were also obtained. Clusters containing PAu?Au?AuP structural motif display good catalytic activity in the activation of alkynes under homogeneous conditions.

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