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2-[(4-chlorophenyl)(piperidin-1-yl)methyl]naphthalen-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1384975-44-3

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1384975-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384975-44-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,9,7 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1384975-44:
(9*1)+(8*3)+(7*8)+(6*4)+(5*9)+(4*7)+(3*5)+(2*4)+(1*4)=213
213 % 10 = 3
So 1384975-44-3 is a valid CAS Registry Number.

1384975-44-3Downstream Products

1384975-44-3Relevant academic research and scientific papers

An amino-naphthol preparation method of compound

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Paragraph 0061; 0062; 0063; 0064, (2017/03/17)

The invention relates to a preparation method for aminonaphthol compound. The method includes the following steps: catalyst, aldehyde compound, secondary amine compound and naphthol are sequentially added into water and react under the temperature condition of 20 DEG C to 80 DEG C, and after reaction is complete, reaction liquid is obtained; the reaction liquid is sequentially extracted, dried, concentrated and separated by column chromatography according to the conventional method, so that product I or product II is obtained, and the structural formula of the product is shown in the figure. The preparation method has the advantages of mild conditions, short reaction time, simple post-processing, high yield and environment-friendliness, can realize mass production and has a good industrial application prospect.

Catalyst-free, one-pot, expeditious synthesis of aminoalkylnaphthols at room temperature

Mukhopadhyay, Chhanda,Rana, Sunil,Butcher, Ray J.

experimental part, p. 3077 - 3088 (2012/07/30)

Aminoalkylnaphthols possess several biological and catalytic activities. A methodology has been developed for the multicomponent one-pot synthesis of aminoalkylnaphthols in dichloromethane under catalyst-free conditions at room temperature. The present ap

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