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furan-2-ylmethyl-(4-nitro-phenyl)-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

647035-69-6

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647035-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 647035-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,7,0,3 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 647035-69:
(8*6)+(7*4)+(6*7)+(5*0)+(4*3)+(3*5)+(2*6)+(1*9)=166
166 % 10 = 6
So 647035-69-6 is a valid CAS Registry Number.

647035-69-6Downstream Products

647035-69-6Relevant academic research and scientific papers

Furfural and 5-(hydroxymethyl)furfural valorization using homogeneous Ni(0) and Ni(II) catalysts by transfer hydrogenation

Arévalo, Alma,García, Juventino J.,Jurado-Vázquez, Tamara

supporting information, (2021/11/27)

The complex [dippeNi(COD)] (dippe =1,2-bis(diisopropyl phosphino)ethane) was used as a catalytic precursor in furfural (FF) and 5-(hydroxymethyl)furfural (HMF) valorization, along with formic acid as hydrogen transfer agent, to produce the corresponding a

Preparative synthesis of 7-carboxy-2-R-isoindol-1-ones

Varlamov,Boltukhina,Zubkov,Sidorenko,Chernyshev,Grudinin

, p. 22 - 28 (2007/10/03)

A preparative method for the synthesis of 7-carboxy-2-R-isoindol-1-ones was developed on the basis of the [4+2] cycloaddition of secondary furfurylamines to maleic anhydride.

Synthesis of Secondary Arylamines through Copper-Mediated Intermolecular Aryl Amination

Okano, Kentaro,Tokuyama, Hidetoshi,Fukuyama, Tohru

, p. 4987 - 4990 (2007/10/03)

(Equation presented) A mild intermolecular copper-mediated amination of aryl iodides has been developed. The reaction takes place at room temperature or heating at 90°C and tolerates halogens attached to the aromatic ring. Its synthetic applications include a synthetic protocol for unsymmetrical N,N′-dialkylated phenylenediamines and both a stepwise and a general synthetic method for N-aryl secondary amines via Ns-anilides (readily obtained by reaction of the Ns-amide).

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