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"N'-(5-nitrofurfurylidene)-3-(5-nitrofurfurylideneamino)benzohydrazide" is a complex organic compound with the chemical formula C15H10N6O6. It is a derivative of furfurylidene, which is a compound derived from furfural, a chemical found in many plants. This specific compound is characterized by the presence of nitro groups (-NO2) attached to the furfuryl rings, which contribute to its chemical properties. It is a yellow crystalline solid and is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique structure and reactivity. The compound's name reflects its structure, indicating that it is a hydrazide with two nitro-furfurylidene groups attached to a central benzene ring.

3524-91-2

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3524-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3524-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3524-91:
(6*3)+(5*5)+(4*2)+(3*4)+(2*9)+(1*1)=82
82 % 10 = 2
So 3524-91-2 is a valid CAS Registry Number.

3524-91-2Downstream Products

3524-91-2Relevant 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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