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25117-74-2

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25117-74-2 Usage

Synthesis Reference(s)

Tetrahedron Letters, 34, p. 1581, 1993 DOI: 10.1016/0040-4039(93)85012-L

Check Digit Verification of cas no

The CAS Registry Mumber 25117-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,1 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25117-74:
(7*2)+(6*5)+(5*1)+(4*1)+(3*7)+(2*7)+(1*4)=92
92 % 10 = 2
So 25117-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO/c1-2-11-9-5-3-8(7-10)4-6-9/h3-6H,2H2,1H3

25117-74-2 Well-known Company Product Price

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  • Alfa Aesar

  • (A19806)  4-Ethoxybenzonitrile, 98%   

  • 25117-74-2

  • 5g

  • 317.0CNY

  • Detail
  • Alfa Aesar

  • (A19806)  4-Ethoxybenzonitrile, 98%   

  • 25117-74-2

  • 25g

  • 1278.0CNY

  • Detail
  • Alfa Aesar

  • (A19806)  4-Ethoxybenzonitrile, 98%   

  • 25117-74-2

  • 100g

  • 4075.0CNY

  • Detail

25117-74-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ETHOXYBENZONITRILE

1.2 Other means of identification

Product number -
Other names Benzonitrile, 4-ethoxy-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25117-74-2 SDS

25117-74-2Relevant articles and documents

Vardenafil analog as well as synthesis method and application thereof

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Paragraph 0059-0064, (2021/11/03)

The vardenafil analog has a brand-new compound structure, is determined in structure and high in chemical purity, and can be used as an impurity reference substance for development and verification of an analysis method of vardenafil hydrochloride. In sub

Mustard Carbonate Analogues as Sustainable Reagents for the Aminoalkylation of Phenols

Annatelli, Mattia,Trapasso, Giacomo,Salaris, Claudio,Salata, Cristiano,Castellano, Sabrina,Aricò, Fabio

supporting information, p. 3459 - 3464 (2021/05/24)

N,N-dialkyl ethylamine moiety can be found in numerous scaffolds of macromolecules, catalysts, and especially pharmaceuticals. Common synthetic procedures for its incorporation in a substrate relies on the use of a nitrogen mustard gas or on multistep syntheses featuring chlorine hazardous/toxic chemistry. Reported herein is a one-pot synthetic approach for the easy introduction of aminoalkyl chain into different phenolic substrates through dialkyl carbonate (β-aminocarbonate) chemistry. This new direct alcohol substitution avoids the use of chlorine chemistry, and it is efficient on numerous pharmacophore scaffolds with good to quantitative yield. The cytotoxicity via MTT of the β-aminocarbonate, key intermediate of this synthetic approach, was also evaluated and compared with its alcohol precursor.

A highly stable all-in-one photocatalyst for aryl etherification: The NiIIembedded covalent organic framework

Chen, Hao,Dong, Wenbo,Hu, Jianxiang,Rao, Li,Wang, Pei,Wang, Shengyao,Xiang, Yonggang,Yang, Yi

, p. 5797 - 5805 (2021/08/23)

The efficient conversion of aryl bromides to the corresponding aryl alkyl ethers by dual nickel/photocatalysis has seen great progress, but difficulties of recycling the photosensitizer or nickel complexes cause problems of sustainability. Here, we report the design of a novel, highly stable vinyl bridge 2D covalent organic framework (COF) containing Ni, which combines the role of photosensitizer and reactive site. The as-prepared sp2c-COFdpy-Ni acts as an efficient heterogeneous photocatalyst for C-O cross coupling. The sp2c-COFdpy-Ni can be completely recovered and used repeatedly without loss of activity, overcoming the limitations of the prior methods. Preliminary studies reveal that strong interlayer electron transfer may facilitate the generation of the proposed intermediate sp2c-COFdpy-NiI in a bimolecular and self-sustained manner. This all-in-one heterogeneous photocatalyst exhibits good compatibility of substrates and tolerance of functional groups. The successful attempt to expand the 2D COFs with this new catalyst into photocatalytic organic transformation opens an avenue for photoredox/transition metal mediated coupling reactions.

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