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5-chloro-N-(5-nitrofurfurylidene)-2-(5-nitrofurfurylideneamino)benzohydrazide is a complex organic chemical compound with the molecular formula C15H8ClN5O5. It is a derivative of furfurylidene, which is a reactive intermediate in the synthesis of various furan-based compounds. This particular compound features a benzohydrazide structure, with two nitro groups attached to the furfurylidene moieties. The presence of the chloro group and the nitro groups imparts unique chemical properties to the molecule, making it potentially useful in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals. Due to its complex structure and functional groups, it is likely to be involved in a variety of chemical reactions, such as nucleophilic substitutions, redox reactions, and condensations. The compound's specific applications and properties would depend on the context in which it is used, and further research would be required to explore its potential uses and reactivity.

3544-03-4

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3544-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3544-03-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3544-03:
(6*3)+(5*5)+(4*4)+(3*4)+(2*0)+(1*3)=74
74 % 10 = 4
So 3544-03-4 is a valid CAS Registry Number.

3544-03-4Downstream Products

3544-03-4Relevant academic research and scientific papers

Modified Procedure for the Preparation of 5-Nitro-2-furylmethylene Diacetate and Its Use in the Synthesis of Some Novel (5-Nitro-2-furyl)azomethines via 5-Nitro-2-furaldehyde

Vlaovic, Djordje,Milic, Bozidar Lj.,Mackenzie, Kenneth

, p. 1201 - 1218 (2007/10/02)

A modified two-step procedure for the preparation of 5-nitro-2-furylmethylene diacetate (3) by nitration of 2-furaldehyde (1) or 2-furylmethylene diacetate (4) with acetyl nitrate via 2-acetoxy-5-nitro-2,5-dihydro-2-furylmethylene diacetate (2), or 1,1,5-triacetoxy-2-hydroxy-5-nitro-3-penten (5) and 1,1,5-triacetoxy-2-hydroxy-5-nitro-2,4-pentadiene (6), has been developed.Acid hydrolysis of 3 yields 5-nitro-2-furaldehyde (7) which is used in the carbonylamine condensation with various hydrazines (9-11, 14, 17, 19, 21, 24, 25, 28, 29, 32, 34, 36, 38, 39, 41 and 44-54) prepared by known methods, in order to obtain some novel potentially pharmaceutically active (5-nitro-2-furyl)azomethines.

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