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1,4-bis-(2,4-dinitro-styryl)-benzene is a complex organic compound with the chemical formula C18H10N4O8. It is characterized by a central benzene ring with two 2,4-dinitrostyryl groups attached at the 1 and 4 positions. Each 2,4-dinitrostyryl group consists of a nitro group (-NO2) at the 2 and 4 positions of a styrene (phenylethylene) unit. This molecule is known for its rigid structure and has been studied for its potential applications in various fields, including materials science and as a chemical intermediate. Due to its nitro groups, it may exhibit explosive properties, and thus, it requires careful handling and storage. The compound's synthesis typically involves the reaction of benzene with 2,4-dinitrostyrene, and it is often used in research settings to explore the properties of polynitro compounds and their potential applications in areas such as explosives and propellants.

2695-78-5

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2695-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2695-78-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,9 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2695-78:
(6*2)+(5*6)+(4*9)+(3*5)+(2*7)+(1*8)=115
115 % 10 = 5
So 2695-78-5 is a valid CAS Registry Number.

2695-78-5Relevant academic research and scientific papers

Application of Phase-Transfer Catalysis to the Synthesis of Mono- and Bis-stilbenes and Styryls

Lokhande, S. B.,Rangnekar, D. W.

, p. 485 - 488 (2007/10/02)

A novel and convenient method has been developed for the synthesis of substituted stilbenes by the condensation of active methyl group in suitably substituted toluenes with aromatic aldehydes in aq. medium at room temperature using benzyltriethylammonium chloride as a phase-transfer catalyst.This method has also been applied for the preparation of heterocyclic styryls and extended to the synthesis of bis-stilbenes and bis-styryls using aromatic dialdehydes in place of monoaldehydes.A comparison of the results shows that the present method is superior to the conventional methods in many respects.

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