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3(5)-Ferrocenylpyrazole is a unique organometallic compound that features a ferrocene moiety attached to a pyrazole ring. Ferrocene, a derivative of cyclopentadienyl anion, is known for its sandwich structure with iron at the center. The pyrazole ring, a five-membered aromatic heterocyclic compound with alternating single and double bonds, is fused to the ferrocene, creating a complex molecule with potential applications in various fields. 3(5)-ferrocenylpyrazole is of interest due to its electronic properties and the possibility of its use in catalysis, materials science, and as a building block for more complex organometallic structures. The combination of the ferrocene's electronic and redox properties with the pyrazole's aromaticity and potential coordination sites makes 3(5)-ferrocenylpyrazole a subject of study for its chemical reactivity and potential applications in advanced materials.

1291-56-1

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1291-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1291-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,9 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1291-56:
(6*1)+(5*2)+(4*9)+(3*1)+(2*5)+(1*6)=71
71 % 10 = 1
So 1291-56-1 is a valid CAS Registry Number.

1291-56-1Downstream Products

1291-56-1Relevant academic research and scientific papers

Synthesis of ferrocenyl pyrazoles by the reaction of (2-formyl-1-chlorovinyl)ferrocene with hydrazines

Zora, Metin,G?rmen, Meral

, p. 5026 - 5032 (2007)

Synthesis of ferrocenyl-substituted pyrazoles via the reaction between (2-formyl-1-chlorovinyl)ferrocene and hydrazine derivatives is described. Depending upon the substitution pattern of hydrazine, the reaction affords 1-alkyl/aryl-5-ferrocenylpyrazoles and/or 1-alkyl/aryl-3-ferrocenylpyrazoles. The reaction appears to be general for a variety of hydrazine derivatives.

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