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Benzeneacetonitrile, 4-nitro-α-[(4-nitrophenyl)methylene]-, also known as 4-nitro-α-(4-nitrobenzylidene)benzeneacetonitrile, is an organic compound with the chemical formula C15H10N2O4. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. Benzeneacetonitrile, 4-nitro-a-[(4-nitrophenyl)methylene]- is characterized by the presence of a benzene ring, a nitrile group, and two nitro groups attached to a benzylidene moiety. It is synthesized through a condensation reaction between 4-nitrobenzaldehyde and benzeneacetonitrile. Benzeneacetonitrile, 4-nitro-a-[(4-nitrophenyl)methylene]- has potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity.

2900-70-1

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2900-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2900-70-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2900-70:
(6*2)+(5*9)+(4*0)+(3*0)+(2*7)+(1*0)=71
71 % 10 = 1
So 2900-70-1 is a valid CAS Registry Number.

2900-70-1Relevant academic research and scientific papers

Highly active g-C3N4 as a solid base catalyst for knoevenagel condensation reaction under phase transfer conditions

Sharma, Priti,Sasson, Yoel

, p. 25589 - 25596 (2017/07/10)

In a promising approach, heterogeneous g-C3N4 as a solid base catalyst exhibits appreciable activity in Knoevenagel condensations at room temperature for the synthesis of substituted stilbene in presence of a crown-ether phase transfer catalyst. High yield of the product substituted stilbene were isolated in a very short reaction time period (~30 min). The solid base g-C3N4 catalyst was proven to be recyclable for several runs. Various aromatic substrates were screened using heterogeneous base g-C3N4 catalyst, exhibiting appreciable corresponding product yield (~99%) at room temperature.

Nucleophilicities of the anions of arylacetonitriles and arylpropionitriles in dimethyl sulfoxide

Kaumanns, Oliver,Appel, Roland,Lemek, Tadeusz,Seeliger, Florian,Mayr, Herbert

supporting information; experimental part, p. 75 - 81 (2009/04/07)

(Chemical Equation Presented) The rates of the reactions of the colored para-substituted phenylacetonitrile anions 1a-c and the pfienylpropionitrile anions 2a-c with Michael acceptors (3a-u) were determined by UV-vis spectroscopy in DMSO at 20°C. The reac

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