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2-amino-4-(3-bromophenyl)-6-(4-hydroxyphenyl)nicotinonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1380592-77-7

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1380592-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380592-77-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,5,9 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1380592-77:
(9*1)+(8*3)+(7*8)+(6*0)+(5*5)+(4*9)+(3*2)+(2*7)+(1*7)=177
177 % 10 = 7
So 1380592-77-7 is a valid CAS Registry Number.

1380592-77-7Downstream Products

1380592-77-7Relevant academic research and scientific papers

Highly efficient four-component synthesis of 2-amino-3-cyanopyridines using doped nano-sized copper(I) oxide (Cu2O) on melamine-formaldehyde resin

Behrouz, Somayeh

, p. 540 - 544 (2016)

A convenient and facile four-component synthesis is described of 2-amino-3-cyanopyridine derivatives from readily available starting materials catalysed by doped nano-sized Cu2O on melamine-formaldehyde resin (nano-Cu2O-MFR). In this method, treatment of different aldehydes, ketones, malononitrile, and ammonium acetate in refluxing H2O/EtOH (1:1) in the presence of doped nano-Cu2O-MFR as a highly efficient heterogeneous catalyst affords the corresponding 2-amino-3-cyanopyridines in good to excellent yields. The nano-Cu2O-MFR is a cheap and stable nano-catalyst that could be easily recovered and reused for many consecutive reaction runs without considerable decrease in its activity.

Ultrasound-promoted an efficient method for one-pot synthesis of 2-amino-4,6-diphenylnicotinonitriles in water: A rapid procedure without catalyst

Safari, Javad,Banitaba, Sayed Hossein,Khalili, Shiva Dehghan

experimental part, p. 1061 - 1069 (2012/07/03)

A green and convenient approach to the synthesis of 2-amino-4,6- diphenylnicotinonitriles via four-component reaction of malononitrile, aromatic aldehydes, acetophenone derivatives and ammonium acetate in water under ultrasound irradiation is described. The combinatorial synthesis was achieved for this methodology with applying ultrasound irradiation while making use of water as green solvent. In comparison to conventional methods, experimental simplicity, good functional group tolerance, excellent yields, short routine, and selectivity without the need for a transition metal or base catalyst are prominent features of this sonocatalyzed procedure.

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