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2-Furancarboxaldehyde, (4-nitrophenyl)hydrazone, also known as 2-furaldehyde-(4-nitrophenyl)hydrazone, is an organic compound with the chemical formula C11H9N3O3. It is a derivative of furan, a heterocyclic aromatic compound, and is formed by the condensation of 2-furancarboxaldehyde with 4-nitrophenylhydrazine. This yellow crystalline solid is used as a reagent in chemical analysis and synthesis, particularly for the detection and determination of aldehydes and ketones. It is soluble in common organic solvents and exhibits a melting point of approximately 198-200°C. Due to the presence of a nitro group, it is sensitive to heat and light, and should be stored in a cool, dark place. The compound is also known for its potential applications in the synthesis of pharmaceuticals and other organic compounds.

3155-21-3

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3155-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3155-21-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3155-21:
(6*3)+(5*1)+(4*5)+(3*5)+(2*2)+(1*1)=63
63 % 10 = 3
So 3155-21-3 is a valid CAS Registry Number.

3155-21-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(E)-furan-2-ylmethylideneamino]-4-nitroaniline

1.2 Other means of identification

Product number -
Other names 2-furaldehyde p-nitrophenylhydrazone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3155-21-3 SDS

3155-21-3Relevant academic research and scientific papers

Synthesis and properties of pyrazolino[60]fullerene-donor systems

Espíldora, Eva,Delgado, Juan Luis,De La Cruz, Pilar,De La Hoz, Antonio,López-Arza, Vicente,Langa, Fernando

, p. 5821 - 5826 (2002)

A series of pyrazolino[60]fullerenes has been prepared in one pot by 1,3-dipolar cycloaddition to C60 of the corresponding nitrile imine, which was generated in situ from the corresponding hydrazone. A range of donors and acceptors were introdu

Solubility of thiophene-, furan- and pyrrole-2-carboxaldehyde phenylhydrazone derivatives in 2.82 mol?L-1 aqueous DMSO at 298.15 K, inhibition of lymphoproliferation and tubulin polymerization: A study based on the scaled particle theory

Alvarado, Ysaías J.,álvarez-Mon, Melchor,Baricelli, Joanna,Caldera-Luzardo, José,Cubillán, Néstor,Ferrer-Amado, Gladys,Hassanhi, Manzur,Marrero-Ponce, Yovani,Mancilla, Victoria,Rocafull, Miguel A.,San?Antonio-Sánchez, Mari?a Esther,Ojeda-Andara, José,Thomas, Luz E.

body text, p. 1099 - 1112 (2011/05/30)

In this work, the solubilities of nine phenylhydrazone derivatives in water and in 2.82 mol ? L-1 aqueous DMSO at 298.15 K, expressed on the molar fraction scale, are reported. The estimated value of the standard Gibbs energy for transferring t

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