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5394-57-0

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5394-57-0 Usage

Uses

2-(4-Methoxyphenoxy)ethanol is a useful compound for preparation of benzannulated and spirobenzannulated compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 5394-57-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5394-57:
(6*5)+(5*3)+(4*9)+(3*4)+(2*5)+(1*7)=110
110 % 10 = 0
So 5394-57-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O3/c1-11-8-2-4-9(5-3-8)12-7-6-10/h2-5,10H,6-7H2,1H3

5394-57-0Relevant articles and documents

Pillar[5]arene-Stabilized Silver Nanoclusters: Extraordinary Stability and Luminescence Enhancement Induced by Host–Guest Interactions

Muhammed, Madathumpady Abubaker Habeeb,Cruz, Laila Khalil,Emwas, Abdul-Hamid,El-Zohry, Ahmed M.,Moosa, Basem,Mohammed, Omar F.,Khashab, Niveen M.

, p. 15665 - 15670 (2019)

Herein, we report the synthesis of a new class of functional silver nanoclusters (AgNCs) capped with pillar[5]arene (P5)-based host ligands. These NCs are readily prepared through direct synthesis or ligand exchange synthesis and are stable at room temper

Synthetic and Mechanistic Studies on 2,3-Dihydrobenzo[ b ][1,4]-oxaselenines Formation from Selenocyanates

Bonesi, Sergio M.,Cattaneo, Mauricio,Chao, María N.,Rodriguez, Juan B.,Sanchez Gonzalez, Jonathan,Szajnman, Sergio H.

, p. 1643 - 1658 (2020/05/25)

An expedient preparation of selenium-containing hetero-cycles via an m -chloroperbenzoic acid-mediated seleno-annulation starting from selenocyanate derivatives is described. In spite of its significance, this cyclization reaction is virtually understudied not only from the point of view of its scope, but also from the mechanistic aspects associated to this remarkable transformation. In this sense, several selenocyanate and thiocyanate derivatives bearing an aromatic ring were evaluated as substrates under different reaction conditions of this interesting cyclization yielding important insights on its scope as well as relevant information on the reaction mechanism.

Copper(ii)-catalyzed c-n coupling of aryl halides and n-nucleophiles promoted by quebrachitol or diethylene glycol

Chen, Guoliang,Chen, Yuanguang,Du, Fangyu,Fu, Yang,Wu, Ying,Zhou, Qifan

supporting information, p. 2161 - 2168 (2019/11/25)

Herein, we report the natural ligand quebrachitol (QCT) as a promoter for a Cu(II) catalyst, which is highly effective for N-Arylation of various amines and related aryl halides. A series of diarylamine derivatives were obtained in high yields by using diethylene glycol (DEG) as both ligand and solvent. The C-N coupling reactions proceed under mild conditions and exhibit good functional group tolerance.

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