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5400-80-6

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5400-80-6 Usage

Chemical Properties

white to light yellow-beige needle-like crystals

Uses

2-Bromo-1-indanol is a bicyclic alcohol with antiviral properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5400-80-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5400-80:
(6*5)+(5*4)+(4*0)+(3*0)+(2*8)+(1*0)=66
66 % 10 = 6
So 5400-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO/c10-8-5-6-3-1-2-4-7(6)9(8)11/h1-4,8-9,11H,5H2/t8-,9+/m0/s1

5400-80-6 Well-known Company Product Price

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  • Alfa Aesar

  • (A13511)  2-Bromo-1-indanol, 99%   

  • 5400-80-6

  • 10g

  • 332.0CNY

  • Detail
  • Alfa Aesar

  • (A13511)  2-Bromo-1-indanol, 99%   

  • 5400-80-6

  • 50g

  • 1149.0CNY

  • Detail
  • Alfa Aesar

  • (A13511)  2-Bromo-1-indanol, 99%   

  • 5400-80-6

  • 250g

  • 4963.0CNY

  • Detail

5400-80-6Relevant articles and documents

Dissymmetric ansa zirconocene complexes with di- and trisubstituted indenyl ligands as catalysts for homogeneous ethylene homo- and ethylene/1-hexene copolymerization reactions

Rimkus, Andrea M.,Alt, Helmut G.

, p. 72 - 82 (2017/02/18)

Different routes for the synthesis of 1,2- and 1,2,3-substituted indene derivatives are described. Representative substituents are: Me, Ph, PhCH2, PhCH2CH2, PhCH2CH2CH2, CH2CH?=?CH2. Subsequent deprotonation of these substituted indenes and reaction with indenyl zirconium trichloride gave the corresponding dissymmetric bis(indenyl) zirconium complexes. After activation with methylaluminoxane (MAO) these complexes show high activities both in ethylene homopolymerisation and ethylene/1-hexene copolymerisation. The rate of comonomer incorporation can reach 33.3% (15/MAO). The copolymers exhibit lower melting points than the homopolymers and their crystallinities α are lower compared with the homopolymers.

On the bromination of aromatics, alkenes and alkynes using alkylammonium bromide: Towards the mimic of bromoperoxidases reactivity

Mendoza, Fabian,Ruíz-Guerrero, Rosario,Hernández-Fuentes, Carlos,Molina, Paulina,Norzagaray-Campos, Mariano,Reguera, Edilso

supporting information, p. 5644 - 5648 (2016/11/28)

This article describes an efficient method of bromination of organic substrates including aromatics, alkenes and alkynes with NH4VO3as a catalyst and H2O2as an oxidant agent using a non-toxic and easy-to-handle source of bromine, tetrabutylammonium bromide. The process was developed under mild reaction conditions and is an innovation from reported methods in aspects such as: i) short reaction times, ii) the ability to work at room temperature, iii) regioselectivity and good yields.

The Activation of Carboxylic Acids via Self-Assembly Asymmetric Organocatalysis: A Combined Experimental and Computational Investigation

Monaco, Mattia Riccardo,Fazzi, Daniele,Tsuji, Nobuya,Leutzsch, Markus,Liao, Saihu,Thiel, Walter,List, Benjamin

supporting information, p. 14740 - 14749 (2016/11/18)

The heterodimerizing self-assembly between a phosphoric acid catalyst and a carboxylic acid has recently been established as a new activation mode in Br?nsted acid catalysis. In this article, we present a comprehensive mechanistic investigation on this activation principle, which eventually led to its elucidation. Detailed studies are reported, including computational investigations on the supramolecular heterodimer, kinetic studies on the catalytic cycle, and a thorough analysis of transition states by DFT calculations for the rationalization of the catalyst structure-selectivity relationship. On the basis of these investigations, we developed a kinetic resolution of racemic epoxides, which proceeds with high selectivity (up to s = 93), giving the unreacted epoxides and the corresponding protected 1,2-diols in high enantiopurity. Moreover, this approach could be advanced to an unprecedented stereodivergent resolution of racemic α-chiral carboxylic acids, thus providing access to a variety of enantiopure nonsteroidal anti-inflammatory drugs and to α-amino acid derivatives.

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