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(4-Methoxy-phenylamino)-(4-nitro-phenyl)-acetonitrile is a complex organic compound with the molecular formula C15H12N2O3. It features a central acetonitrile group (CH3CN), which is bonded to two distinct aryl groups: a 4-methoxy-phenyl group and a 4-nitro-phenyl group. The 4-methoxy-phenyl group contains a methoxy substituent (-OCH3) at the para position, while the 4-nitro-phenyl group has a nitro group (-NO2) at the para position. (4-Methoxy-phenylamino)-(4-nitro-phenyl)-acetonitrile is characterized by its unique structure, which combines electron-donating and electron-withdrawing groups, potentially influencing its reactivity and properties. It may be of interest in chemical research and pharmaceutical applications due to its specific functional groups and structural features.

38565-11-6

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38565-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38565-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,6 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38565-11:
(7*3)+(6*8)+(5*5)+(4*6)+(3*5)+(2*1)+(1*1)=136
136 % 10 = 6
So 38565-11-6 is a valid CAS Registry Number.

38565-11-6Downstream Products

38565-11-6Relevant academic research and scientific papers

Sulfamic acid catalyzed direct condensation of aldehydes, amines, and TMSCN to α-aminonitriles at ambient temperature

Li, Zhenjiang,Sun, Yingjie,Ren, Xinghua,Wei, Ping,Shi, Yuhu,Ouyang, Pingkai

, p. 803 - 805 (2007/12/25)

A simple and efficient method has been developed for the synthesis of α-aminonitriles by a one-pot three-component condensation of aldehydes, amines, and trimethylsilyl cyanide in the presence of a catalytic amount of sulfamic acid at room temperature. Georg Thieme Verlag Stuttgart.

Organocatalytic activation of TMSCN by basic ammonium salts for efficient cyanation of aldehydes and imines

Raj, I. Victor Paul,Suryavanshi, Gurunath,Sudalai

, p. 7211 - 7214 (2008/03/11)

Basic ammonium salts act as highly effective catalysts for the cyanosilylation of aldehydes and in Strecker-type aminonitrile synthesis using TMSCN as cyanide source at 25 °C under extremely mild conditions, affording very good to excellent yields of silylated cyanohydrins and α-aminonitriles.

Cu(OTf)2 or Et3N-catalyzed three-component condensation of aldehydes, amines and cyanides: a high yielding synthesis of α-aminonitriles

Paraskar, Abhimanyu S.,Sudalai, Arumugam

, p. 5759 - 5762 (2007/10/03)

Copper(II) triflate or Et3N have been found to catalyze, under ambient conditions, the addition of a cyanide anion, such as trimethylsilyl cyanide or acetone cyanohydrin, onto in situ generated imines, furnishing α-aminonitriles in excellent yi

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