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1-benzyl-1H-indol-6-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161460-28-2

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161460-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161460-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,4,6 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 161460-28:
(8*1)+(7*6)+(6*1)+(5*4)+(4*6)+(3*0)+(2*2)+(1*8)=112
112 % 10 = 2
So 161460-28-2 is a valid CAS Registry Number.

161460-28-2Downstream Products

161460-28-2Relevant academic research and scientific papers

Catalyst-free Synthesis of 6-Hydroxy Indoles via the Condensation of Carboxymethyl Cyclohexadienones and Amines

Reddy, Reddy Rajasekhar,Adlak, Komalkant,Ghorai, Prasanta

, p. 8426 - 8437 (2017)

An efficient catalyst-free synthesis of 6-hydroxy indoles from carboxymethyl cyclohexadienones and primary amines has been developed. The aza-Michael addition of the in situ formed enamine, generated through the condensation of carboxymethyl unit of the s

A catalytic oxidation fragrant boron class compound preparing phenol method (by machine translation)

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Paragraph 0073; 0105; 0106, (2017/08/08)

The invention discloses a method for catalytic oxidation of phenolic compounds fragrant boron class compound synthesis method, the flux in the solvent in the aqueous solution, under the action of alkali, adding hydrazine hydrate or acid hydrazides catalyst, catalytic oxidation fragrant boron class compound directly for the preparation of phenolic compound. The invention of the method of preparation of the phenol compound, the catalyst is a cheap hydrazine hydrate or hydrazine compound, the oxidizing agent is atmospheric pressure of air or oxygen, the reaction does not need good and activeness metal catalyst, is extensive and stable substrate, substrate-sensitive functional group compatibility good and wide range of application. In the optimized under the reaction conditions, the yield of the target product separation up to 99%. (by machine translation)

Palladium-catalyzed hydroxylation of aryl and heteroaryl halides enabled by the use of a palladacycle precatalyst

Cheung, Chi Wai,Buchwald, Stephen L.

, p. 5351 - 5358 (2014/06/23)

A method for the hydroxylation of aryl and heteroaryl halides, promoted by a catalyst based on a biarylphosphine ligand tBuBrettPhos (L5) and its corresponding palladium precatalyst (1), is described. The reactions allow the cross-coupling of both potassium and cesium hydroxides with (hetero)aryl halides to afford a variety of phenols and hydroxylated heteroarenes in high to excellent yield.

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